Abstract: The invention relates to a process for the preparation of anilines which are m-substituted by chlorine, by selective dehalogenation of more highly chlorinated anilines in an acid medium in the presence of noble metal catalysts and in the presence of optionally substituted phenols.The 3-chloro- or 3,5-dichloroanilines obtainable by the process according to the invention are known intermediate products, and can be used for the preparation of plant protection agents.
Type:
Grant
Filed:
June 16, 1982
Date of Patent:
July 17, 1984
Assignee:
Bayer Aktiengesellschaft
Inventors:
Karlfried Wedemeyer, Ferdinand Hagedorn, Werner Evertz
Abstract: A process for the preparation of thiuram disulfides substituted with aliphatic cycloaliphatic, araliphatic, or aromatic hydrocarbon radicals, said process comprising reacting a suitably substituted secondary amine having a pK.sub.a .gtoreq.8 with carbon disulfide in a solvent and in the presence of oxygen or oxygen-containing gas, a solvent, and a metalliferous catalyst, at a temperature of between 0.degree. C. and 200.degree. C.
Type:
Grant
Filed:
February 16, 1982
Date of Patent:
July 10, 1984
Assignee:
Akzona Incorporated
Inventors:
Ludwig Eisenhuth, Hans G. Zengel, Manfred Bergfeld
Abstract: A method for conducting transesterification reactions employing a catalyst system comprising metallic sodium and aluminum isopropoxide which provides a facile, high yield, means for producing compounds such as esters of alkyl- and alkyloxy-substituted arylamines.
Abstract: This invention relates to novel polyprenyl ketone derivatives having the eral formula: ##STR1## in which n is an integer of 1-5, and R represents a hydroxymethyl, formyl or carboxyl group, and a process for the preparation of the same.
Type:
Grant
Filed:
October 16, 1981
Date of Patent:
June 26, 1984
Assignees:
Eisai Co., Ltd., General Director of the Agency of Industrial Science and Technology
Abstract: This disclosure describes symmetrical 1,4-bis(substituted-amino)-5,8-dihydroxyanthraquinones useful as chelating agents and for inhibiting the growth of transplanted mouse tumors.
Abstract: Phosphoramide derivatives of the general formula: ##STR1## are disclosed wherein X and Y each represents a hydrogen atom or X and Y are removed to form a double bond between the respective adjoining carbon atoms, and n represents an integer of 0 to 2. A process for the preparation of these compounds and pharmaceutical compositions containing these phosphoramide derivatives are also disclosed. The phosphoramide derivatives of the invention are used to treat urethral calculosis and pyelonephritis.
Abstract: The invention relates to a process for the continuous manufacture of azo pigments, wherein a coupling component is reacted, inside a reaction zone filled with a previously produced suspension of the azo pigment to be made, with an aqueous solution of a diazo component at 10.degree. to 60.degree. C. and over periods of 0.2 to 4 hours.
Type:
Grant
Filed:
October 9, 1979
Date of Patent:
June 12, 1984
Assignee:
Hoechst Aktiengesellschaft
Inventors:
Hartmut Behringer, Kurt Karrenbauer, Heinrich Rehberg
Abstract: Olive oil is recovered from olives by separating olive pits from olives to obtain a pitless olive meat, by maintaining the pitless olive meat at a temperature of about 70.degree. F. to about 110.degree. F., by introducing the pitless olive meat to an extraction zone, by withdrawing a liquid phase comprising olive oil, water, and a minor proportion of pulp from a first portion of the extraction zone, and by withdrawing a substantially dry solid olive pulp from a second portion of the extraction zone. The pulp and water are separated from the oil to obtain a pure olive oil. An inert additive is mixed with the pitless olive meat before extraction to increase the yield of product olive oil. Where olive culls are used as the starting material, the culls are wetted before the pits are separated.
Type:
Grant
Filed:
February 4, 1982
Date of Patent:
June 5, 1984
Assignee:
FPS Development Partnership
Inventors:
Harvey E. Finch, Salvatore P. Trapanese
Abstract: A compound represented by the following formula ##STR1## wherein R represents a lower alkyl group having 2 to 6 carbon atoms, and n is an integer of from 1 to 5.
Abstract: Cyclohexenes of the formula ##STR1## wherein R.sup.1 is hydroxy or lower alkoxy; n is 1 or 2; R.sup.2 is lower alkyl; and R.sup.3 is hydrogen, lower alkyl, lower alkenyl or lower cycloalkylmethyl,and their pharmaceutically acceptable acid addition salts are disclosed. The compounds of formula I have analgesic activity and are useful for the control of pains.
Type:
Grant
Filed:
March 24, 1982
Date of Patent:
May 15, 1984
Assignee:
Hoffmann-La Roche Inc.
Inventors:
Hans Bruderer, Albert E. Fischli, Rudolf Pfister
Abstract: Hydroxybenzenes are converted to the corresponding amines by contacting the hydroxybenzene and ammonia at temperatures of about 250.degree.-550.degree. C. and pressures of about 0-5000 psig with a novel siliceous composition prepared by impregnating porous silica with aluminum hydride and subsequently heating the impregnated silica to a temperature of from about 300.degree. C. to about 900.degree. C. in a non-oxidizing environment.
Abstract: The invention relates to new 2-ketosulfonamides of the general formula ##STR1## and to a process for their preparation, which process comprises oxidizing compounds of the general formulaR--CHOH--CH.sub.2 --SO.sub.2 NH.sub.2with manganese dioxide in a readily volatile, oxidation-stable organic solvent, preferably acetone or acetonitrile.
Abstract: There is provided herbicidal arylsulfonamide derivatives of phenoxybenzoic acids. These compounds are particularly useful when applied in a post-emergence application to soybean fields containing broadleaf weeds.
Abstract: Substituted bromofluorobenzene, wherein the fluorine is in para-position and the bromine in meta-position to another substituent, is prepared by direct bromination of the corresponding fluorobenzene derivative. Bromination is advantageously carried out in the presence of a catalyst, preferably a metal or metal salt. The elementary bromine is used in an amount of 0.9 to 1.3 mols per mol of fluorobenzene derivative and the reaction temperature is between 20.degree. and 200.degree. C. The bromofluorobenzene derivatives are suitable for the synthesis of medicaments and plant protective agents.
Abstract: Process for the production of carnitine amide in the form of a chloride. The carnitine ethyl ester is obtained by reaction of 4-chloroacetoacetic acid ethyl ester with trimethyl amine and the subsequent hydrogenation is carried out with the help of a Pt/C catalyst. Such carnitine ethyl ester, without isolating it, is reacted with ammonia in an autoclave at -30.degree. to +10.degree. C. Everything is heated to 40.degree. to 80.degree. C. The mixture is stirred at such temperature at an ammoniac pressure of 8 to 24 atu. The product is filtered after cooling it to ambient temperature and counterbalancing the excess pressure. The product is then washed with alcohol and subsequently dried at 30.degree. to 50.degree. C. and at a pressure of 15 to 25 torr.
Abstract: Carbon monoxide - containing gas streams are passed over a catalyst to deposit a surface layer of active surface carbon thereon essentially without the formation of inactive coke. The active carbon is subsequently reacted with steam or hydrogen to form methane. Surprisingly, hydrogen and water vapor present in the feed gas do not adversely affect CO utilization significantly, and such hydrogen actually results in a significant increase in CO utilization.
Abstract: Immiscible components are controllably released into aqueous systems by impregnating silica-silicate open cell foams with the immiscible components. As the silica-silicate foams are gradually dissolved, the immiscible components are released. Fragrance oils and dyes are particularly adaptable for use in the invention. In fact, silica-silicate foams impregnated with fragrance oils having polar functional groups, exhibit an unexpectedly slower rate of dissolution into aqueous environments and consequently, fragrance oils and dyes admixed therewith are released in aqueous systems over extended time periods.
Abstract: This invention relates to S-alkylcysteines and processes for preparing same. The compounds according to this invention are expected to be applicable as therapeutic agents for hepatic failures.
Abstract: Water-insoluble azo dyestuffs, their manufacture and use, which have the formula ##STR1## wherein D is a substituted phenyl or heterocyclic moiety which are free from ionic substituents and R.sup.1 is methyl or ethyl.
Type:
Grant
Filed:
April 24, 1981
Date of Patent:
April 3, 1984
Assignee:
Cassella Aktiengesellschaft
Inventors:
Horst Tappe, Rudolf Lowenfeld, Uwe Kosubek, Maria Kallay