Abstract: An alkane and/or cycloalkane thiol is converted to disulfide with oxygen or air in presence of a catalyst system comprising a cobalt molybdate-alkali metal- and/or an alkaline earth metal hydroxide. A solvent, e.g., an alcohol or an alcohol-water mixture is employed. In one embodiment, 2-methyl-2-propane thiol (tertiary-butyl mercaptan) is converted.
Abstract: 2,2'-Bisphenol sulfoxides are prepared by oxidizing 2,2'-bisphenol sulfides with hydrogen peroxide in the presence of such an organic solvent as not to form any organic peracids under reaction conditions.
Abstract: Disclosed is a method of synthesizing a polyol (allyl carbonate) by the alkali metal hydroxide catalyzed reaction of allyl alcohol and a polyol chloroformate where a portion of the alkali metal hydroxide is anhydrous.
Abstract: Tricyclic isoindole derivatives characterized by having a 1,2,3,4,6,10b-hexahydropyrazino[2,1-a]isoindole or 1,3,4,10b-tetrahydropyrimido[6,1-a]isoindol-6(2H)-one nucleus are disclosed. The foregoing compounds are useful antihypertensive agents.
Type:
Grant
Filed:
September 24, 1979
Date of Patent:
June 16, 1981
Assignee:
American Home Products Corporation
Inventors:
Christopher A. Demerson, Leslie G. Humber, Jean-Marie Ferland
Abstract: Compounds of the formula ##STR1## wherein R is aliphatic hydrocarbyl, alicyclic hydrocarbyl or aryl suitably substituted, if desired, or a heterocyclic group, R.sup.1 is hydrogen or alkyl, R.sup.2 is alkyl or alkoxy, R.sup.3 is ##STR2## wherein a is 0 or 1, R.sup.4 is hydrogen or CW'.sub.3, the W' being hydrogen or halogen, Z is halogen and X is halogen, hydroxy, alkoxy, acetoxy, carbethoxyalkoxy, phenoxy, alkylthio, carbethoxyalkylthio, phenylthio, phosphono, dithiophosphonoxy, phosphoramido, isocyanato, isothiocyanato, alkyl- and dialkylthiocarbamoylthio, alkyl- and dialkylcarbamoyloxy, alkylsulfonyl, etc., have herbicidal activity.
Abstract: A method for making aromatic ether imides is provided by effecting the displacement of reactive radicals on a phthalimide nucleus with a mono- or bis-alkali metal phenoxide in the presence of a nonpolar solvent and a phase transfer catalyst, such as a tetra-ammonia salt. The aromatic ether imides made by the present invention are useful intermediates for making aromatic ether anhydrides and aromatic bis(ether anhydrides).
Abstract: A novel class of compounds which are useful as plant growth regulators has the general structural formula ##STR1## in which R is H or CH.sub.3, R' is halogen, trifluoromethyl, cyano or C.sub.1 to C.sub.3 alkyl or alkoxy and n is zero or an integer from 1 to 2.The compounds are synthesized by reacting a compound of the formula ##STR2## with an isocyanate of the formula ##STR3## under basic conditions in a non-reactive, polar organic solvent.
Abstract: The novel compound (3-nitro-4-methyl)-phenyl chloroformate is prepared by reacting (4-methyl)-phenyl chloroformate with nitric acid in the presence of sulfuric acid.The novel compound (3-nitro-4-methyl)-phenyl chloroformate is a valuable starting material for the preparation of dyes and crop protection agents and in particular is an intermediate for the preparation of 3-nitro-4-methylphenol, which is reduced to 3-amino-4-methylphenol.
Abstract: The compounds according to the invention have the formula I ##STR1## in which R.sup.1, R.sup.2 and R.sup.3 are monovalent organic radicals or chlorine and Z is a tetravalent organic radical and A is a divalent organic grouping. These products are to be used as adhesion promoters, especially between inorganic solids and organic resins. 4 processes of preparation are given.
Abstract: The novel bis (2-bromoethyl) tellurium dibromide and 2-bromoethyl tellurium tribromide are prepared by reacting ethylene with a source of tellurium tetrabromide in an inert, non-basic organic solvent under certain temperature conditions and in the substantial absence of molecular oxygen.
Abstract: The novel hydroquinone derivatives of the formula (I) are useful intermediates for the preparation of coenzyme Q, vitamin K and the polyprenyltrimethylquinones: ##STR1## wherein R.sup.1 is lower alkyl, lower alkoxy lower alkyl or methoxyethoxymethyl, R.sup.2 and R.sup.3 are each methyl or methoxy, or R.sup.2 and R.sup.3, taken together with the carbon atoms from which they depend, define a benzene ring, and R.sup.4 is a substituted or unsubstituted aromatic hydrocarbon. The compounds (I) are readily prepared either by reacting a Grignard reagent of the formula (II) with a halosulfone (III) in the presence of a copper compound, or by reacting a copper derivative (II') of the Grignard reagent (II) with a halo-sulfone (III), as follows: ##STR2## wherein R.sup.1, R.sup.2, R.sup.3 and R.sup.4 are defined as above, and X is a halogen atom or a tosyl group.
Abstract: A compound of the formula: ##STR1## wherein R.sub.1 and R.sub.2, which may be the same or different, are each a C.sub.1 -C.sub.3 alkyl group, a chloromethyl group or a halogen atom, R.sub.3 is a hydrogen atom, a methyl group or a halogen atom, n is an integer of 2 to 5 and X is a hydrogen atom, a methyl group, a methoxy group or a chlorine atom, which is useful as a herbicide.
Abstract: Magnetic substances in particles of a diameter in the range between 1 and 20 nm are suspended in the physiological solution by which cells are loaded with materials when their cell membranes have increased permeability, the magnetic materials being provided in such dosing, that when the cells are loaded, separated from the loading solution and prepared for use in a fresh physiological solution, thereafter injected to a living body, they can be collected and held fast at a predetermined location, for example, at the location of a tumor, by the effect of an external magnetic field. Ferritin, magnetite, cobalt ferrite, nickel ferrite and other ferrimagnetic, ferromagnetic or even paramagnetic compounds can be incorporated into loaded cells for this purpose.
Type:
Grant
Filed:
December 12, 1977
Date of Patent:
May 26, 1981
Assignee:
Kernforschungsanlage Julich Gesellschaft mit beschrankter Haftung
Abstract: The preparation of (.+-.)-9-[.alpha.-(2.alpha.,3.beta.-dihydroxy-4.alpha.-(hydroxymethyl)cycl opentyl)]-6-substituted purines: ##STR1## and (.+-.)-3-[.alpha.-(2.alpha.,3.beta.-dihydroxy-4.alpha.-(hydroxymethyl)cycl opentyl)]-7-substituted-v-triazolo[4,5d]pyrimidines: ##STR2## and their derivatives wherein R is amino, mercapto, methylmercapto, hydroxy, halogen, or substituted amino: ##STR3## wherein R' and R" may be the same or different and are of hydrogen, methyl, ethyl, propyl or phenyl. The preparation of the single intermediate from which either of these series of compounds may be synthesized is also disclosed. The compounds exhibit antiviral and antitumor activity. Acid salts and esters of the purine nucleosides have also been prepared.
Type:
Grant
Filed:
January 5, 1979
Date of Patent:
May 19, 1981
Assignee:
The Regents of the University of Minnesota
Abstract: 4-(Arylaliphatic)isoxazoles, having antiviral activity, are prepared by reacting with hydroxylamine a diketone of the formula Ar-Y-CH(CO-R).sub.2, wherein Ar is substituted phenyl, Y is (CH.sub.2).sub.n or O(CH.sub.2).sub.n, and R is lower-alkyl.
Abstract: Thioethers may be prepared by reacting a thiol, such as thiophenol, with an alcohol (having electron donor groups in the alpha or beta position to its hydroxyl group) such as phenyl-1-hydroxy-phenethylsulfide. Reaction is carried out in the presence of a Lewis Acid metal halide, typically zinc chloride.
Abstract: Covers polyester polycarbonates of the structure: ##STR1## wherein X and Y, independently, are H, methyl, or ethyl, m and n independently are integers of 1-5, R is a nucleus of a glycol selected from the group of lower alkylene glycols and polyalkylene glycols of up to about 600 molecular weight, Z is an organic radical from a cyclic organic acid anhydride having 4-20 carbon atoms, and r is an integer of 1-5.Also covers a method of preparing said polyester polycarbonates as well as polyurethanes derived therefrom, as well as polyisocyanurate polymers containing both isocyanurate linkages and urethane linkages.
Abstract: Perfluoroalkyl compounds containing ether groups have the formulaR.sub.f R.sub.1 SCH.sub.2 CH.sub.2 O T Zwherein R.sub.f is a perfluoroalkyl, R.sub.1 is alkylene or alkyleneoxy or aminoalkylene, T is alkylene, and Z is hydrogen; hydroxy; NR.sub.3 R.sub.4, where R.sub.3 and R.sub.4 each is alkyl or together with nitrogen form a heterocyclic ring; N.sup.+ R.sub.3 R.sub.4 (R.sub.5)X.sub.z.sup.-y, where R.sub.5 is hydrogen, oxide, alkyl, or substituted alkyl, X is an anion, and y is 1 or 2; z is 0 or 1 or is --OCH.sub.2 CH.sub.2 SR.sub.1 R.sub.f ; can be prepared directly by free-radical catalyzed addition of a perfluoroalkylthiol to a vinyl ether or subsequent reaction. These compounds are useful as surfactants and oil spill collecting agents.
Abstract: 2,4,5-Trichloropyrimidine is obtained by reacting 2-cyanoethyl isocyanide dichloride with hydrogen chloride and then reacting the product with chlorine.
Type:
Grant
Filed:
November 30, 1979
Date of Patent:
May 5, 1981
Assignee:
Bayer Aktiengesellschaft
Inventors:
Fritz Doring, Gunther Beck, Gerhard Dankert
Abstract: A novel class of compounds which are useful as plant growth regulators is disclosed, having the general structural formula: ##STR1## in which R.sup.1 is; C.sub.1 to C.sub.4 alkyl, nitro or halo and n is zero or an integer from 1 to 4R.sup.2 and R.sup.3 are; H or C.sub.1 to C.sub.4 alkyl or hydroxyalkyl, or benzyl andAr is; adamantyl, C.sub.3 to C.sub.4 alkyl or alkenyl, benzyl, halobenzyl, naphthyl, phenyl or phenyl bearing thereon from one to three of the substituents: cyano, benzyloxy, methylenedioxy, nitro, bromo, chloro, trifluoromethyl and C.sub.1 to C.sub.4 alkyl, alkenyl, alkoxy, alkylthio and alkyl-substituted amino.