Abstract: A novel process allows a simple preparation of highly pure halogen-substituted dibenzyl alcohols by reduction of the corresponding halogen-substituted terephthalic acids and reaction with an alkylating agent, sulfuric acid, alkyl- or arylsulfonic acids. The highly pure halogen-substituted dibenzyl alcohols obtained are suitable in particular for preparing pharmaceutically or agrochemically active compounds.

Abstract: The present invention is directed to labeled compounds, specifically where each C* is selected from the group consisting of a carbon-12, i.e., 12C, or a carbon-13, i.e., 13C and at least one C* is 13C, R1 is selected from the group of C1-C4 lower alkyl and aryl, and X is selected from the group of —NR2R3 where R2 and R3 are each independently selected from the group of C1-C4 lower alkyl, alkoxy and aryl, —SR4 where R4 is selected from the group of C1-C4 lower alkyl, alkoxy and aryl, and —OR5 where R5 is selected from the group of C1-C4 lower alkyl, alkoxy and aryl with the proviso that when R1 is methyl then R5 is other than methyl, when R1 is ethyl then R5 is other than ethyl, and when R1 is benzyl then R5 is other than benzyl.

Abstract: There is described the preparation of phenylphenol compounds of formula (1) by reaction of a keto compound of formula (3) with dioxolane of formula (4) and with an ammonium compound of formula (5) to from &bgr;-aminoketone compound of formula (6) (reaction step (I)), reaction of the compound of formula (6) with a compound of formula (7) to form a compound of formula (2) (reaction step (II)), and subsequent alkylation to form a compound of formula (1) (reaction step (III)) in accordance with scheme (A); wherein R1, R2, R3, R6 and R7 are each independently of the others hydrogen or C1-C8alkyl; R4, R5 and R8 are each independently of the others hydrogen or C1-C5alkyl; ant Hal is a halogen atom. The compounds prepared in accordance with the invention are suitable as antimicrobial active substances.

Abstract: A process for the preparation of optically pure acetylenediols of the formulae R-I and S-I and their further reaction to give meso-zeaxanthin are described.

Abstract: The invention disclosed in this application relates to a process for the preparation of xanthophyll crystals containing at least 85% total xanthophylls with at least 90% trans-lutein and/or zeaxanthin, trace amounts of cis-lutein and other carotenoids which comprises admixing and heating xanthophyll ester concentrate using excess alcoholic alkali solution, maintaining the resulting mixture at a temperature in the range of 65.degree.C. to about 80.degree C.

Abstract: A process for the preparation of optically pure acetylenediols of the formulae R-I and S-I and their further reaction to give meso-zeaxanthin are described.

Abstract: There is disclosed a process for producing bisphenol A by subjecting phenol and acetone to condensation reaction in the presence of a catalyst composed of an acid type ion exchange resin which is modified in part with a sulfur-containing amine compound, wherein the ion exchange resin having a modification rate of 10 to less than 20 mol % is used for a methanol concentration in acetone of lower than 250 ppm by weight, and the ion exchange resin having a modification rate of 20 to 65 mol % is used for a methanol concentration in acetone of 250 to 8000 ppm by weight. The above process is capable of producing bisphenol A at high conversion and selectivity by suppressing deterioration of catalytic activity due to methanol as an impurity in acetone.

Abstract: The method for preparing 2,2,3,4,4,4-hexafluoro-1-butanol includes reacting methanol and hexafluoropropene in the presence of a free radical initiator such as di-isopropyl peroxydicarbonate at 25-50° C. and a pressure of 100-300 psi in an autoclave. An inert gas such as nitrogen and argon is added to the autoclave when the pressure is lower than 100 psi in the course of the reaction.

Abstract: The present invention provides a method for extracting carotenoids from green plant materials using supercritical fluid extraction. A first and second supercritical fluid extraction is performed on the green plant composition at two different pressures to obtain two extracts. The first extract includes substantial amounts of &bgr;-carotene. The second extract is substantially free of &bgr;-carotene, and includes substantial amounts of lutein.

Abstract: In the production of bisphenol A by condensation of phenol and acetone with the use of a cation exchange resin as a catalyst and optionally a free mercaptan as a promoter, the degree of conversion of phenol is maintained by increasing the molar ration of acetone/phenol with the deterioration of the cation exchange resin; with this method, bisphenol A can be effectively produced with industrial advantage.

Abstract: Compounds containing carbodiimide units and carboxyl or carboxylate groups (compounds V), derived from a) aliphatic or araliphatic C4 to C20 polyisocyanates (component a) b) amino carboxylic acids or amino carboxylic salts (component b) and c) if desired, further compounds which carry groups able to react with isocyanate groups in an addition reaction (component c) d) if desired, other isocyanates (component d), the carbodiimide units deriving essentially exclusively from the isocyanate groups of component (a).

Abstract: There is disclosed a process for producing bisphenol A by continuously supplying phenol to a first-stage reactor in a continuous multi-stage fixed-bed reaction system composed of at least two reactors each filled in with a cation exchange resin as a catalyst, and continuously supplying acetone separately to each of the reactors, characterized by arranging a reactor which is filled in with a fresh or regenerated cation exchange resin on the final stage in the case of replacing the most seriously deteriorated cation exchange resin in catalytic activity with the fresh or regenerated cation exchange resin, and operating the final stage reactor so that the ratio R of the feed rate of acetone to the consumption rate thereof falls within more than one to less than 3. The above process makes it possible to efficiently produce bisphenol A having favorable hue, while maintaining the acetone feed rate at a relatively low level.

Abstract: A process for the preparation of a solution of a quaternary cation and an anion from a deprotonated hydroxy aromatic in an organic solvent by means of a reactive extraction of a quaternary salt in the presence of an aqueous hydroxide solution, a hydroxy aromatic and an organic solvent is disclosed. Also disclosed is a process for the recycling of a quaternary salt phenolate solution from a reaction mixture.

Abstract: Monodisperse cation-exchangers and anon-exchangers are conditioned by a process and thereafter used as catalysts and for the production of bisphenols.

Abstract: A process for the production of 2,2-bis(4-hydroxyphenyl)propane (BPA) is disclosed. The process that entails reacting acetone with phenol in the presence of cross-linked sulfonated polystyrene resins is characterised in that BPA is separated from the reaction solution downstream of the reaction unit by means of a multi-stage vacuum distillation and a subsequent single- or multi-stage layer crystallisation. The by-product stream with accumulated by-products is returned downstream of the reaction unit.

Abstract: Hydroxyphenyl adamantanes are represented by the general formula (1): wherein R is an alkyl group, cycloalkyl group or phenyl group; m is 0 or an integer 1 or 2; l is 0 or 1; when l is 1, hydroxy groups of substituted hydroxyphenyl groups at positions 1 and 3 are together in para-position; n is 0 or an integer 1, 2 or 3; and when l is 0, n is an integer 1, 2 or 3.

Abstract: The invention relates to a process for preparing phenol derivatives by catalytic oxidation of an aromatic hydrocarbon to the hydroperoxide and subsequent cleavage of the hydroperoxide to give the phenol derivative and a ketone, wherein a compound of the formula I where R1, R2=H, aliphatic or aromatic alkoxy radical, carboxyl radical, alkoxycarbonyl radical or hydrocarbon radical, in each case having from 1 to 20 carbon atoms, SO3H, NH2, OH, F, Cl, Br, I and/or NO2, where R1 and R2 are identical or different radicals or R1 and R2 may be joined to one another via a covalent bond, and X, Z=C, S, CH2 Y=O, OH k=0, 1, 2 l=0, 1, 2 m=1-3; is used as oxidation catalyst in the presence of a free-radical initiator, where the molar ratio of the catalyst to the aromatic hydrocarbon is less than 10 mol %.

Abstract: There is provided a process for the manufacture of phenolic compounds by separating a neutralized aralkyl hydroperoxide cleavage mass stream containing salts of neutralization into a crude ketone stream and a crude phenolic stream containing the salts of neutralization; separating the crude phenolic stream into a concentrated phenolic-rich stream, enriched in phenolic compounds, and a crude phenolic bottoms stream enriched in tars and alpha methyl styrene dimers, each compared to the crude phenolic stream, said crude phenolic bottoms stream containing salts of neutralization; to the crude phenolic bottoms stream, adding water and a diluent composition, thereby forming a phase separable crude phenolic bottoms stream, said diluent composition comprised of hydrocarbons phase compatible with the crude phenolic bottoms stream and having a combined density lower than the density of the crude phenolic bottoms stream; separating the separable crude phenolic bottoms stream into a hydrocarbon phase and an aqueous phase

Abstract: Disclosed are a method of producing p-hydroxyphenylalkanol of formula(I): wherein R1 and R2 independently represent hydrogen, an alkyl or a phenyl which may be substituted with an alkyl, or the like, R3, R4, R5, R6 and R7 independently represent hydrogen, an alkyl or the like and n denotes an integer from 0 to 7, the method being characterized in that a phenol compound of formula (II): wherein R1 and R2 respectively represent the aforementioned meaning, is reacted with an unsaturated alcohol of formula (III): R3R4C═C(R5)—C(R6)(R7)—(CH2)n—OH  (III) wherein R3, R4, R5, R6, R7 and n respectively represent the same as defined above, in the presence of (A) at least one compound selected from the group consisting of alkali metals, alkali metal compounds, alkaline earth metals and alkaline earth metal compounds and (B) at least one compound selected from the group consisting of transition metals and transition metal compounds, and the like.

Abstract: A method of producing a chemical reaction is provided. In the practice of one embodiment of the invention, the method includes the steps of providing a reaction vessel and reactants; placing at least one of the reactants in the reaction vessel; and allowing the reaction to proceed for a time interval. A volume increment of at least one of the reactants is withdrawn from the reaction vessel, and a volume increment of at least one of the reactants is added to the reaction vessel. The volume increment withdrawal/addition is repeated after successive time intervals until the reaction reaches a substantially steady state. In various alternative embodiments, the volume increment withdrawal can take place before, after, or contemporaneously with the volume increment addition.