Process for the oxidation of secondary amines into the corresponding nitroxides
The invention relates to a process for the preparation of secondary nitroxide radicals from their corresponding secondary amines by oxidation with an organic peracid, comprising the steps a) adding to a reaction vessel a secondary amine, optionally together with an organic solvent and in one batch a base selected from the group consisting of alkali metal, alkaline earth metal or ammonium bicarbonates and alkaline earth metal or ammonium carbonates or mixtures thereof in the form of a solid together with water or as an aqueous slurry; b) dosing a peracid under stirring to the reaction mixture in an amount of 1.0 to 2.5 mol per mol of secondary amine; and c) isolating the organic phase.
Nitroxides, in particular nitroxides of 2,2,6,6-tetraalkyl piperidine, are a very important class of compounds for various industrial applications. They are, for example, used as inhibitors to prevent premature polymerization of vinyl aromatic monomers during purification and distillation. They are also known as efficient stabilizers for organic materials, such as for thermosetting or thermoplastic polymers. Further applications for nitroxides are oxidation catalysts, polymerization regulators in controlled radical polymerization processes and spin labeling agents.
Numerous methods exists for their preparation. Some are for example described in L. B. Volodarsky, V. A. Reznikov, V. I. Ovcharenko: “Synthetic Chemistry of Stable Nitroxides”, CRC Press, Boca Raton, 1994. Oxidation of suitable secondary amines is among the most versatile ones.
Different oxidants can be used. From an industrial point of view, hydrogen peroxide, optionally together with various catalysts, t-butylhydroperoxide or peracids, in particular peracetic acid, are useful oxidants.
Peracids bring about a fast and often quantitative oxidation of the amine. They are particularly suitable for the oxidation of amines, which are difficult or impossible to oxidize with hydrogen peroxide, for example of highly sterically hindered amines.
One important parameter for the successful oxidation with a peracid is the pH of the reaction mixture. Thus, if the pH is too low, the oxidation may become too slow because the amine is exhaustively protonated. On the other side, if the pH is raised too much by the addition of a strong base such as e.g. sodium hydroxide, the peracid may decompose under evolution of O2. This leads to the failure of the oxidation and poses additionally a serious security risk, as the oxygen may form an explosive mixture with possibly present volatile organic compounds. In WO 00/40550 it is suggested to solve this problem by adding simultaneously together with the peracid to the reaction mixture an aqueous solution of for example an alkali metal carbonate or bicarbonate. Peracid and base are simultaneously added as aqueous solutions to the stirred emulsion of water and amine, which is pre-dissolved in an appropriate organic solvent. The dosing rates of peracid and base are regulated in such a way that the pH is maintained in the range of 4 to 12.
Although this is a feasible method, such mode of operation gives raise to serious drawbacks:
a) The apparatus must be equipped with two dosing units.
b) Measuring of the pH is required. However, a reliable pH-measurement in heterogeneous mixtures is rather difficult, in particular in large scale production,
c) Alkali metal bicarbonates have a rather low solubility in water. As a consequence, large volumes of solutions are required. Therefore, the volume yield is low, which negatively influences the economics of the operation.
These drawbacks make the prior art process less attractive for large-scale industrial oxidation processes.
The instant invention avoids these drawbacks and allows thus a substantially more efficient process, particularly when large-scale production is envisaged.
The invention relates to a process for the preparation of secondary nitroxide radicals from their corresponding secondary amines by oxidation with an organic peracid, comprising the steps
a) adding to a reaction vessel a secondary amine, optionally together with an organic solvent and in one batch a base selected from the group consisting of alkali metal, alkaline earth metal or ammonium bicarbonates and alkaline earth metal or ammonium carbonates or mixtures thereof in the form of a solid together with water or as an aqueous slurry;
b) dosing a peracid under stirring to the reaction mixture in an amount of 1.0 to 2.5 mol per mol of secondary amine; and
c) isolating the organic phase.
Adding a base in one batch according to the invention means, that the total amount is added in one single batch, in contrast to dosing it in small portions.
Preferably the organic solvent used in step a) is immiscible with water.
Examples are aromatic solvents, saturated hydrocarbon solvents or ketones.
The peracid may be any organic peracid, for example performic, peracetic, perpropionic, perbenzoic, m-chlorperbenzoic or trifluoroperacetic acid. Preferred is peracetic acid. The peracid may be used pure or in a suitable solvent. Preferred is the solution of peracetic acid in water or in acetic acid.
Preferably the amount of water added in step a) is sufficient to dissolve the organic acid salt formed in the neutralization reaction between the organic acid and the bicarbonate or carbonate.
The overall oxidation reaction is represented by the following equation:
>N—H+1.5 RCOOOH→>N—O*+1.5 RCOOH+0.5 H2O
The buffering bases of the present invention are for example bicarbonates of alkali metals and alkaline earth metals (group 1+2 elements) or ammonium bicarbonate or carbonates of alkaline earth metals (group 2 elements) or ammonium carbonate. Mixed salts such as for example dolomite CaCO3×MgCO3 can also be used.
The bicarbonates or carbonates may also be partially replaced by alkaline metal hydroxides or alkaline earth metal hydroxides, for example sodium hydroxide, calcium hydroxide or magnesium hydroxide.
Useful are for example also basic carbonates of alkaline earth metals of a general formula nMCO3×mM(OH)2 n, m are integers between 1-10.
The buffering process consists of a partial or complete neutralization of the formed acid RCOOH according for example to:
n RCOOH+M(HCO3)n→(RCOO)nM+n CO2+n H2O
when M is an alkali metall cation (Li+, Na+, K+, . . . ) or NH4+, then n=1
when M is an alkaline earth metall cation (Ca++, Mg++, . . . ), then n=2
Or if an alkaline earth metal carbonate, for example CaCO3, is used:
2 RCOOH+MCO3→(RCOO)2M+CO2+H2O
The minimal volume of water in the process disclosed in WO 00/40550) for a given amount of bicarbonate is determined by its solubility in water at the given temperature. On the other hand, no or only little water is needed in the process of the present invention. Conveniently, a minimal amount of water may be added in the process of the present invention to ensure the formation of a homogeneous aqueous layer of the neutralized acids. Its amount is for example given by the solubility of the corresponding salts resulting from the organic peracid, for example acetates, if peracetic acid is used.
For example, when sodium bicarbonate (NaHCO3) is used as base, the weight ratio of NaHCO3 to water is typically from 1.5:1 to 0.75:1.
The carbonates of alkaline earth metals, such as for example CaCO3, MgCO3 or Dolomite (CaCO3×MgCO3) have such a low solubility in water that usefully concentrated solutions cannot be prepared. Thus, these carbonates would lead to an extremely low volume yield in the process disclosed in WO 00/40550.
A considerable further advantage of the above mentioned weak bases is that their aqueous slurries do not trigger fast decomposition of the peracid. The difficult measurement of pH in a heterogeneous reaction system is therefore not necessary in the instant process. It is, however, mandatory in the prior art process.
To illustrate this, the solubility data of the technically most important bicarbonates and acetates are presented in Table 1.
ag/100 g Water. (CRC Handbook of Chemistry and Physics, 82 nd Edition)
bg/100 g Solution. (R. K. Freier: “Aqueous Solutions”, Walter de Gruyter, Berlin 1976)
Table 2 shows the minimal amount of water, calculated with the data from Table 1, which is needed for the preparation of a solution of 1 mol of bicarbonate to be dosed according to WO 00/40550.
The minimal amount of water needed to completely dissolve the acetate formed during the neutralization of 1 mol acetic acid with 1 mol of bicarbonate or 0.5 mol of carbonate loaded as a solid according to the present invention into the reactor is calculated for comparison. The water formed during the neutralization is not taken into consideration.
Table 2 clearly shows that the amount of the reactor volume occupied by the unproductive aqueous phase is substantially reduced in the process according to the present invention.
For example the base is sodium or potassium bicarbonate, calcium or magnesium carbonate or dolomite.
Special preference is given to sodium or potassium bicarbonate.
For instance the base is added in an amount of from 0.1 to 1.5 equivalent base per 1 equivalent of all acids present, for example from 0.5 to 1.3.
A suitable reaction temperature is between −20° C. and 80° C., preferably between 0° C. and 40° C.
Conveniently the dosage of the peracid is carried out from 10 minutes to 5 hours.
The total reaction time is for example from 30 minutes to 10 hours. The reaction is carried out, for Instance, at atmospheric pressure.
The nitroxide radical formed is for example of formula (I)
Rp and Rq are independently tertiary bound C4-C28alkyl groups or C3-C17 secondary bound alkyl groups which are unsubstituted or substitituted by one or more electron withdrawing groups or by phenyl; or
Rp and Rq together form a 5, 6 or 7 membered heterocyclic ring which is substituted at least by 4 C1-C4alkyl groups and which may be interrupted by a further nitrogen or oxygen atom.
Consequently the secondary amine precursor is of formula (I′)
The amine precursors are mostly items of commerce.
The nitroxyl radicals and their secondary amine precursors are principally known from U.S. Pat. No. 4,581,429 or EP-A-621 878. Particularly useful are the open chain compounds described in WO 98/13392, WO 99/03894 and WO 00/07981, the piperidine derivatives described in WO 99/67298 and GB 2335190 or the heterocyclic compounds described in GB 2342649 and WO 96/24620.
Further suitable nitroxylethers and nitroxyl radicals are described in WO 02/4805 and WO 02/100831
Examples of nitroxyl radicals, which can be prepared by the instant process are given below. For example the nitroxyl radical contains a structural element of formula (X)
wherein
G1, G2, G3, G4 are independently C1-C6alkyl or G1 and G2 or G3 and G4, or G1 and G2 and G3 and G4 together form a C5-C12cycloalkyl group;
*denotes a valence; and
G5, G6 independently are H or C1-C6alkyl.
Consequently the amine precursor is of formula (X′)
For instance the nitroxide radical is of formula A′, B′ or O′,
wherein
m is 1,
R is hydrogen, C1-C18alkyl which is uninterrupted or interrupted by one or more oxygen atoms, cyanoethyl, benzoyl, glycidyl, a monovalent radical of an aliphatic carboxylic acid having 2 to 18 carbon atoms, of a cycloaliphatic carboxylic acid having 7 to 15 carbon atoms, or an, -unsaturated carboxylic acid having 3 to 5 carbon atoms or of an aromatic carboxylic acid having 7 to 15 carbon atoms;
p is 1;
R101 is C1-C12alkyl, C5-C7cycloalkyl, C7-C8aralkyl, C2-C18alkanoyl, C3-C5alkenoyl or benzoyl;
R102 is C1-C18alkyl, C5-C7cycloalkyl, C2-C8alkenyl unsubstituted or substituted by a cyano, carbonyl or carbamide group, or is glycidyl, a group of the formula —CH2CH(OH)-Z or of the formula —CO-Z or —CONH-Z wherein Z is hydrogen, methyl or phenyl;
G5 and G6 are independently hydrogen or C1-C4alkyl, and
G1 and G3 are methyl and G2 and G4 are ethyl or propyl or G1 and G2 are methyl and G3 and G4 are ethyl or propyl.
More preferably in formula A′, B′ and O′
R is hydrogen, C1-C18alkyl, cyanoethyl, benzoyl, glycidyl, a monovalent radical of an aliphatic, carboxylic acid;
R101 is C1-C12alkyl, C7-C8aralkyl, C2-C18alkanoyl, C3-C5alkenoyl or benzoyl;
R102 is C1-C18alkyl, glycidyl, a group of the formula —CH2CH(OH)-Z or of the formula —CO-Z,
wherein Z is bydrogen, methyl or phenyl.
The above compounds, their precursors and their preparation are for example described in GB 2335190 and GB 2 361 235. Some are commercially available.
Another group of nitroxyl radicals are those of formula (Ic′), (Id′), (Ie′), (If′), (Ig′) or (Ih′)
wherein R201, R202, R203 and R204 independently of each other are C1-C18alkyl, C3-C18alkenyl, C3-C18alkinyl, C1-C18alkyl, C3-C18alkenyl, C3-C18alkinyl which are substituted by OH, halogen or a group —O—C(O)—R205, C2-C18alkyl which is interrupted by at least one O atom and/or NR205 group, C3-C12cycloalkyl or C6-C10aryl or R201 and R202 and/or R203 and R204 together with the linking carbon atom form a C3-C12cycloalkyl radical;
R205, R206 and R207 independently are hydrogen, C1-C18alkyl or C6-C10aryl;
R208 is hydrogen, OH, C1-C18alkyl, C3-C18alkenyl, C3-C18alkinyl, C1-C18alkyl, C3-C18alkinyl which are substituted by one or more OH, halogen or a group —O—C(O)—R205, C2-C18alkyl which is interrupted by at least one O atom and/or NR205 group, C3-C12cycloalkyl or C6-C10aryl, C7-C9phenylalkyl, C5-C10heteroaryl, —C(O)—C1-C18alkyl, —O—C1-C18alkyl or —COOC1—C18alkyl; and
R209, R210, R211and R212 are independently hydrogen, phenyl or C1-C18alkyl.
More preferably in formula (Ic′), (Id′), (Ie′), (If′), (Ig′) and (Ih′) at least two of R201, R202, R203 and R204 are ethyl, propyl or butyl and the remaining are methyl; or
R201 and R202 or R203 and R204 together with the linking carbon atom form a C5-C6cycloalkyl radical and one of the remaining substituents is ethyl, propyl or butyl.
The above compounds, their precursors and their preparation is described in GB 2342649.
Other suitable compounds are the 4-imino piperidine derivatives of formula V
wherein
G11, G12, G13 and G14 are independently C1-C4alkyl or G11 and G12 together and G13 and G14 together, or G11 and G12 together or G13 and G14 together are pentamethylene;
G15 and G16 are each independently of the other hydrogen or C1-C4alkyl;
k is1, 2, 3, or 4
Y is O, NR302 or when n is 1 and R301 represents alkyl or aryl Y is additionally a direct bond;
R302 is H, C1-C18alkyl or phenyl;
if k is 1
R301 is H, straight or branched C1-C18alkyl, C3-C18alkenyl or C3-C18alkinyl, which may be unsubstituted or substitued, by one or more OH, C1-C8alkoxy, carboxy, C1-C8alkoxycarbonyl;
C5-C12cycloalkyl or C5-C12cycloalkenyl;
phenyl, C7-C9phenylalkyl or naphthyl which may be unsubstituted or substituted by one or more C1-C8alkyl, halogen, OH, C1-C8alkoxy, carboxy, C1-C8alkoxycarbonyl;
—C(O)—C1-C36alkyl, or an acyl moiety of a, -unsaturated carboxylic acid having 3 to 5 carbon atoms or of an aromatic carboxylic acid having 7 to 15 carbon atoms;
—SO3−Q+, —PO(O−Q+)2, —P(O)(OR2)2, —SO2—R2, —CO—NH—R2, —CONH2, COOR2, or Si(Me)3,
wherein Q+ is H+, ammnonium or an alkali metal cation;
if k is 2
R301, is C1-C18alkylene, C3-C18alkenylene or C3-C18alkinylene, which may be unsubstituted or substitued, by one or more OH, C1-C8alkoxy, carboxy, C1-C8alkoxycarbonyl;
or xylylene; or
R301 is a bisacyl radical of an aliphatic dicarboxylic acid having 2 to 36 carbon atoms, or a cycloaliphatic or aromatic dicarboxylic acid having 8-14 carbon atoms;
if k is 3,
R301 is a trivalent radical of an aliphatic, cycloaliphatic or aromatic tricarboxylic acid; and
if k is 4, R301 is a tetravalent radical of an aliphatic, cycloaliphatic or aromatic tetracarboxylic acid.
The compounds are described in WO 02/100831.
Preferably G16 is hydrogen and G15 is hydrogen or C1-C4alkyl, in particular methyl, and G11 and G13 are methyl and G12 and G14 are ethyl or propyl or G11 and G12 are methyl and G13 and G14 are ethyl or propyl.
The alkyl radicals in the various substituents may be linear or branched. Examples of alkyl containing 1 to 18 carbon atoms are methyl, ethyl, propyl, isopropyl, butyl, 2-butyl, isobutyl, t-butyl, pentyl, 2-pentyl, hexyl, heptyl, octyl, 2-ethylhexyl, t-octyl, nonyl, decyl, undecyl, dodecyl, tridecyl, tetradecyl, hexadecyl and octadecyl.
Alkenyl with 3 to 18 carbon atoms is a linear or branched radical as for example propenyl, 2-butenyl, 3-butenyl, isobutenyl, n-2,4-pentadienyl, 3-methyl-2-butenyl, n-2-octenyl, n-2-dodecenyl, iso-dodecenyl, oleyl, n-2-octadecenyl oder n-4-octadecenyl.
Preferred is alkenyl with 3 bis 12, particularly preferred with 3 to 6 carbon atoms.
Alkinyl with 3 to 18 is a linear or branched radical as for example propinyl (—CH2—C≡CH), 2-butinyl, 3-butinyl, n-2-octinyl, oder n-2-octadecinyl. Preferred is alkinyl with 3 to 12, particularly preferred with 3 to 6 carbon atoms.
Examples for hydroxy substituted alkyl are hydroxy propyl, hydroxy butyl or hydroxy hexyl.
Examples for halogen substituted alkyl are dichloropropyl, monobromobutyl or trichlorohexyl.
C2-C18alkyl interrupted by at least one O atom is for example —CH2—CH2—O—CH2—CH3, —CH2—CH2—O—CH3— or —CH2—CH2—O—CH2—CH2—CH2—O—CH2—CH3—. It is preferably derived from polyethlene glycol. A general description is —((CH2)a—O)b—H/CH3, wherein a is a number from 1 to 6 and b is a number from 2 to 10.
C2-C18alkyl interrupted by at least one NR5 group may be generally described as —((CH2)a—NR5)b—H/CH3, wherein a, b and R5 are as defined above.
C3-C12cycloalkyl is typically, cyclopropyl, cyclopentyl, methylcyclopentyl, dimethylcyclopentyl, cyclohexyl, methylcyclohexyl or trimethylcyclohexyl.
C6-C10 aryl is for example phenyl or naphthyl, but also comprised are C1-C4alkyl substituted phenyl, C1-C4alkoxy substituted phenyl, hydroxy, halogen or nitro substituted phenyl. Examples for alkyl substituted phenyl are ethylbenzene, toluene, xylene and its isomers, mesitylene or isopropylbenzene. Halogen substituted phenyl is for example dichlorobenzene or bromotoluene.
Alkoxy substituents are typically methoxy, ethoxy, propoxy or butoxy and their corresponding isomers.
C7-C9phenylalkyl is benzyl, phenylethyl or phenylpropyl.
C5-C10heteroaryl is for example pyrrol, pyrazol, imidazol, 2, 4, dimethylpyrrol, 1-methylpyrrol, thiophene, furane, furfural, indol, cumarone, oxazol, thiazol, isoxazol, isothiazol, triazol, pyridine, α-picoline, pyridazine, pyrazine or pyrimidine.
If R is a monovalent radical of a carboxylic acid, it is, for example, an acetyl, propionyl, butyryl, valeroyl, caproyl, stearoyl, lauroyl, acryloyl, methacryloyl, benzoyl, cinnamoyl or β-(3,5-di-tert-butyl-4-hydroxyphenyl)propionyl radical.
C1-C18alkanoyl is for example, formyl, propionyl, butyryl, octanoyl, dodecanoyl but preferably acetyl and C3-C5alkenoyl is in particular acryloyl.
Specific examples are:
Most preferred are the following compounds:
The compounds mentioned above or their amine precursors are partially commercially available or they are prepared by known methods. Higher alkyl substituted piperidines and their preparation are for example described in GB 2 335 190 and in GB 2 361 235. The following examples illustrate the invention.
EXAMPLE 1 Oxidation of 2,6-Diethyl-2,3,6-trimethyl-piperidine-4-one Using CH3COOOH/CaCO3A four neck flask equipped with stirrer, thermometer and dropping funnel is charged with powdered calcium carbonate (20 g, 0.2 mol), water (75 ml), toluene (30 ml) and 2,6-diethyl-2,3,6-trimethyl-piperidine-4-one (19.73 g, 0.1 mol, prepared as described in Ger. Offen. DE 2623422). Peracetic acid (30.4 g, 0.16 mol, 40% solution in acetic acid) is then added dropwise over 50 minutes to the stirred mixture while keeping the temperature between 20-30° C. The mixture is then stirred for additional 150 minutes. The red organic layer is separated, washed with saturated NaHCO3 and water, dried over MgSO4 and evaporated to yield 19.26 g of 2,6-diethyl-2,3,6-trimethyl-piperidin-4-one-N-oxyl as a red liquid. The material is identical with the sample prepared as described in DE 19909767.
EXAMPLE 2 Oxidation of 2,6-Diethyl-2,3,6-trimethyl-piperidine-4-one Using CH3COOOH/MgCO3Magnesium carbonate (12.65 g, 0.15 mol) is employed in the same manner as described in example 1, using only 35 ml of water to yield 21.1 g of 2,6-diethyl-2,3,6-trimethyl-piperidine-4-one-N-oxyl as a red liquid. The material is identical with the sample prepared as described in DE 19909767.
EXAMPLE 3 Oxidation of 2,6-Diethyl-2,3,6-trimethyl-piperidine-4-one Using CH3COOOH/4MgCO3×Mg(OH)2×5H2OThe mixed magnesium carbonate-hydroxide of the formula 4MgCO3×Mg(OH)2×5H2O (Fluka) (14.56g, 0.03 mol) is employed In the same way as described in example 2 to yield 20.25 g of 2,6-diethyl-2,3,6-trimethyl-piperidine4-one-N-oxyl as a red liquid. The material is identical with the authentic sample prepared as described in DE 19909767.
EXAMPLE 4 Oxidation of 2,6-Diethyl-2,3,6-trimethyl-piperidin-4-one Using CH3COOOH/NH4HCO3Ammonium bicarbonate (23.72g, 0.3 mol) is employed in the same way as described in example 1 using only 20 ml of water to yield 20.52 g of 2,6-diethyl-2,3,6-trimethyl-piperidine-4-one-N-oxyl as a red liquid. The material is identical with the authentic sample prepared as described in DE 19909767.
EXAMPLE 5 Oxidation of 2,6-Diethyl-2,3,6-trimethyl-piperidine-4-one Using CH3COOOH/KHCO3Potassium bicarbonate (30.03g, 0.3 mol) is employed in the same way as described in example 1 using only 11 ml of water and 30 ml of ethyl acetate instead of toluene to yield 20.77 g of 2,6-diethyl-2,3,6-trimethyl-piperidine4-one-N-oxyl as a red liquid. The material is identical with the authentic sample prepared as described in DE 19909767.
EXAMPLE 6 Oxidation of 2,6-Diethyl-2,3,6-trimethyl-piperidine using CH3COOOH/NaHCO3A four neck flask equipped with stirrer, thermometer and dropping funnel is charged with sodium bicarbonate (25.20 g, 0.3 mol), water (25 ml), ethylacetate (25 ml) and 2,6-diethyl-2,3,6-trimethyl-piperidine (9.17 g, 0.05 mol, prepared as described in WO 00 46202). Peracetic acid (19.01 g, 0.1 mol, 40% solution in acetic acid) is then added dropwise over 50 minutes to the stirred mixture while keeping the temperature between 20-30 ° C. The mixture is then stirred for additional 10 hours. The red organic layer is separated, washed with saturated NaHCO3 and water, dried over Na2SO4 and evaporated to yield 9.63 g of 2,6-diethyl-2,3,6-trimethyl-piperidine-N-oxyl as a red liquid. The material is identical with the authentic sample prepared as described in DE 2621841.
EXAMPLE 7 Oxidation of 2,2,6,6-Tetramethylpiperidin-4-one Using CH3COOOH/NaHCO3A four neck flask equipped with stirrer, thermometer and dropping funnel is charged with sodium bicarbonate (101.8 g, 1.2 mol), water (100 ml), ethylacetate (100 ml) and 2,2,6,6-tetramethylpiperidin-4-one (31.05 g, 0.2 mol, Aldrich). Peracetic acid (19.01 g, 0. mol, 40% solution in acetic acid) is then added dropwise over 50 minutes to the stirred mixture while keeping the temperature between 20-30 ° C. The mixture is then stirred for additional 30 minutes. The reaction mass is transferred into a separatory funnel, water (500 ml) is added and the red organic layer is separated. The aqueous layer is extracted with ethyl acetate (2×200 ml). The extracts and the organic layer are combined, dried over Na2SO4 and evaporated. The oily residue is crystallized from 50 ml hexane to yield 29.6 g of 2,2,6,6-tetramethylpiperidin-4-one-N-oxyl as a red solid. The material is identical with the authentic sample obtained from Aldrich.
EXAMPLE 8 Oxidation of Octadecanoic Acid 3,8,10-triethyl-7,8,10-trimethyl-1,5-dioxa-9-aza-spiro-[5.5]undec-3-ylmethyl ester Using with CH3COOOH/NaHCO3To a stirred solution of 31.35 g (0.1 mol) 3,8,10-triethyl-7,8,10-trimethyl-1,5-dioxa-9-aza-spiro[5.5]undec-3-yl)-methanol (prepared as described in U.S. Pat. No. 4,105,626) in 48 g of toluene were slowly added 30.3 g (0.1 mol) of stearoyl chloride while keeping the temperature between 91-96° C. The mixture after the addition is stirred at room temperature for 12 h. The stirrer is stopped, and the solution of sodium hydroxide (4.2 g, 0.105 mol) in 15 ml water is added at once to the reaction mixture, which is then vigorously stirred for 5 minutes. Then, 25.2 g (0.3 mol) of solid NaHCO3 are added to the reaction mixture. Thereafter, 30.45 g (0.16 mol) of peracetic acid, 40% in acetic acid, are added dropwise within 65 minutes. The inner temperature is kept between 24-33° C. The red emulsion is then stirred at 24° C. for additional 3.5 hours. The red organic layer is transferred into a separatory funnel and is washed twice with 25 ml of deionized water, dried over MgSO4 and evaporated on a rotary evaporator to give 59.35 g (99.7%) of the targeted nitroxide as a red oil.
Elemental analysis: C36H68NO5 (594.95), C: 72.62/72.63% (theory: 72.68%), H: 11.35/11.46% (theory: 11.52%), N: 2.25/2.22% (theory: 2.35%).
Claims
1. A process for the preparation of secondary nitroxide radicals from their corresponding secondary amines by oxidation with an organic peracid, comprising the steps
- a) adding to a reaction vessel a secondary amine, optionally together with an organic solvent, and in one batch a base selected from the group consisting of alkali metal, alkaline earth metal or ammonium bicarbonates and alkaline earth metal or ammonium carbonates or mixtures thereof in the form of a solid together with water or as an aqueous slurry;
- b) dosing a peracid under stirring to the reaction mixture in an amount of 1.0 to 2.5 mol per mol of secondary amine; and
- c) isolating the organic phase.
2. A process according to claim 1 wherein the organic solvent optionally used in step a) is immiscible with water.
3. A process according to claim 1 wherein the peracid is peracetic acid.
4. A process according to claim 1 wherein the amount of water added in step a) is sufficient to dissolve the organic acid salt formed in the neutralization reaction between the organic acid and the bicarbonate or carbonate.
5. A process according to claim 1 wherein the base is sodium or potassium bicarbonate, calcium or magnesium carbonate or dolomite.
6. A process according to claim 1 wherein the base is added in an amount of from 0.1 to 1.5 equivalents base per 1 equivalent of all acids present.
7. A process according to claim 1 wherein the reaction temperature is between 0° C. and 40° C.
8. A process according to claim 1 wherein the dosage of the peracid is carried out from 10 minutes to 5 hours.
9. A process according to claim 1 wherein the nitroxide radical is of formula (I)
- Rp and Rq are independently tertiary bound C4-C28alkyl groups or C3-C17 secondary bound alkyl groups which are unsubstituted or substitituted by one or more electron withdrawing groups or by phenyl; or
- Rp and Rq together form a 5, 6 or 7 membered heterocyclic ring which is substituted at least by 4 C1-C4alkyl groups and which may be interrupted by a further nitrogen or oxygen atom.
10. A process according to claim 1 wherein the nitroxide radical contains a structural element of formula (X) wherein
- G1, G2, G3, G4 are independently C1-C6alkyl or G. and G2 or G3 and G4, or G1 and G2 and G3 and G4 together form a C5-C12cycloalkyl group;
- * denotes a valence; and
- G5, G6 independently are H or C1-C6alkyl.
Type: Application
Filed: Mar 17, 2004
Publication Date: Oct 12, 2006
Inventors: Peter Nesvadba (Marly), Lucienne Bugnon (Pfeffingen), Martin Von Büren (Muttenz)
Application Number: 10/549,526
International Classification: C07D 211/40 (20060101);
