Abstract: New chemical compounds are derivatives of certain substituted 1,4-napthoquinones in which the keto oxygens at the 4-positions have been replaced by certain cyanoalkoxycarbonylmethylene groups. The new compounds have the structure ##STR1## wherein: J is alkyl having 1 to 6 carbon atoms, andR is normal alkyl having 1 to 6 carbon atoms.The compounds are useful as electron-transport agents in electrophotographic elements.
Type:
Grant
Filed:
December 21, 1988
Date of Patent:
March 20, 1990
Assignee:
Eastman Kodak Company
Inventors:
Teh-Ming Kung, William B. Vreeland, Ralph H. Young
Abstract: Organic iodine compounds are separated from carbonylation products of methanol, methyl acetate and dimethyl ether and from mixtures of such carbonylation products by a process wherein the iodine compounds are removed by liquid phase extraction with a non-aromatic hydrocarbon.
Abstract: Compounds of Formula I ##STR1## the pharmaceutically acceptable salts, and the gamma-lactone form thereof are described. They are antagonists of leukotrienes and SRS-A.
Abstract: An improved process for producing 2-methyl-1,4-naphthoquinone with a high yield comprising reaction of a 1-lower-alkoxy-2-methyl naphthalene with hydrogen peroxide in the presence of a hexacyanoferric acid or a salt thereof as catalyst. This process does not employ hazardous chromium compounds unlike conventional methods.
Abstract: New chlorinated .beta.-ketoesters of the formula: ##STR1## wherein R represents alkyl of 1 through 6 carbon atoms or alkenyl of 2 through 6 carbon atoms, and R.sub.1 represents alkyl of 1 through 4 carbon atoms, their preparation and their use for the preparation of ethylenic ketones of the formula: ##STR2## wherein R is as hereinbefore defined.
Abstract: Aqueous bischloroformates are prepared by the reaction of a dihydroxyaromatic compound (e.g., bisphenol A) with phosgene in a substantially inert organic liquid (e.g., methylene chloride) and in the presence of an aqueous alkali metal or alkaline earth metal base, at a pH below about 8. After all solid dihydroxyaromatic compound has been consumed, the pH is raised to a higher value in the range of about 7-12, preferably 9-11, and maintained in said range until a major proportion of the unreacted phosgene has been hydrolyzed. At the same time, any monochloroformate in the product may be converted to bischloroformate.
Abstract: Aqueous glyoxylic acid solutions, essentially free of other acids, are recovered from aqueous solutions which still contain other acids, by a method in which the aqueous solution is mixed with an organic nitrogen compound at as high as 50.degree. C., the phases are separated, and the glyoxylic acid is extracted from the organic phase with water, at a higher temperature.
Type:
Grant
Filed:
October 18, 1984
Date of Patent:
February 20, 1990
Assignee:
BASF Aktiengesellschaft
Inventors:
Gerhard Wickenhaeuser, Bernd Heida, Fritz Graf, Leopold Hupfer
Abstract: Disclosed is an improved process for the preparation of adipic acid by the air oxidation of cyclohexane in the presence of acetic acid and a catalyst system comprising cobalt and zirconium and/or hafnium.
Type:
Grant
Filed:
May 3, 1988
Date of Patent:
February 20, 1990
Assignee:
Eastman Kodak Company
Inventors:
Guy R. Steinmetz, Norma L. Lafferty, Charles E. Sumner, Jr.
Abstract: An asymmetric synthesis for Vitamin E in an optically active pure form for 4-(2,5-diloweralkanoyloxy)-3,4,6-trimethylphenyl-butan-2-one and intermediates therein.
Abstract: This invention relates to a process for producing a fluorinated ester containing a trifluoromethyl group by esterification in the presence of .gamma.-butyrolactone as a solvent, and more particularly a process or producing a fluorinated ester containing a trifluoromethyl group which is useful as a raw material of various fluorine containing compound.
Abstract: Compounds of the formula: ##STR1## wherein l is an integer of 0 to 18, X is hydrogen, an alkyl having 1 to 4 carbon atoms or a carboxylic acyl having 2 to 4 carbon atoms and Y is a phenylene, a cycloalkylene having 3 to 7 carbon atoms or a group of the formula: ##STR2## in which m is an integer of 0 to 3, and R.sub.1 and R.sub.2 each is an alkyl having 1 to 4 carbon atoms, are novel compounds, possess circulatory disturbance-improving activity and inhibitory activity of the generation and release of SRS-A, and used for prophylactic or therapy of ischemic diseases such as cerebral apoplexy or allergic diseases.
Abstract: This invention produces higher homologs, i.e., differing by at least a --CH.sub.2 -unit, of carbonyloxy-containing compounds by treating the carbonyloxy-containing compounds with carbon monoxide and hydrogen in the presence of a ruthenium-containing compound, a proton donor, an iodide promoter, and optionally, a manganese-containing compound.
Type:
Grant
Filed:
May 1, 1981
Date of Patent:
January 30, 1990
Assignee:
Union Carbide Chemicals and Plastics Company Inc.
Abstract: The invention relates to a new crystalline calcium salt of valproic acid, in which per molecule 5 valproic acid radicals are associated with one calcium ion. The salt is non-hygroscopic and has superior galenic characteristics as active agent in pharmaceutical preparations, particularly for oral application.The calcium salt is useful for the treatment of epilepsy and febrile convulsions.
Abstract: Fatty acid and their derivatives are simply produced by reacting an olefin, carbon monoxide and water or reacting an alcohol or its derivative and carbon monoxide in the presence of a hydrogen fluoride catalyst and thermally decomposing the resulting reaction product in the presence of a lower hydrocarbon or a lower halogenated hydrocarbon.
Abstract: A process for treating carbonylation catalyst solutions which contain a rhodium component and a lithium component to remove metallic corrosion products comprises contacting the catalyst solution with a cation exchange resin in the lithium form.
Type:
Grant
Filed:
October 14, 1986
Date of Patent:
January 16, 1990
Assignee:
Hoechst Celanese Corporation
Inventors:
Mark O. Scates, G. P. Torrence, Ronny G. Wood
Abstract: Disclosed are alpha-acyloxyketone derivatives which are useful as intermediates for production of N-cyano-N'-methyl-N"-[2-{(5-methyl-1H-imidazol-4-yl)methylthio}ethyl]guani dine (common name: Cimetidine; Cimetidine applies hereinafter) and Cimetidine-related compounds which have an action of controlling secretion of gastric acid and are useful as a drug for treating gastric ulcer.
Type:
Grant
Filed:
December 28, 1987
Date of Patent:
January 16, 1990
Assignee:
Mitsui Petrochemical Industries, Ltd.
Inventors:
Hiroaki Tan, Koji Kato, Junichi Imuta, Noriaki Kihara
Abstract: A process is disclosed for producing N-acetyl-aminoacid which comprises reacting a feedstock from the group consisting of simple olefins, acetamide and synthesis gas with a catalyst comprising a cobalt-containing compound promoted by a bidental-phosphine ligand in a solvent at a pressure of 500 psi or greater and a temperature of 50.degree. C. or greater. The presence of the ligand increases both reaction rate and cobalt catalyst stability.
Abstract: Improved acid yield and product quality are realized in the oxidation of aromatic hydrocarbons in a two-stage process, employing an aqueous solvent system and an increased proportion of bromine, and, optionally, of catalytic metals, in the second stage.
Abstract: The invention is concerned with a novel process for the manufacture of compounds of the formula ##STR1## wherein R.sup.1 signifies C.sub.1-5 -alkyl, especially methyl, ethyl, propyl or isopropyl, and the radicals R.sup.2 each independently represent hydrogen or C.sub.1-5 -alkyl, especially hydrogen or methyl, ethyl, propyl or isopropyl.The process is characterized in that a compound of the formula ##STR2## wherein R stands for C.sub.1-4 -alkoxy, chlorine, bromine or C.sub.1-4 -alkanoyloxy, R.sup.1 and R.sup.2 have the above significance and R.sup.3 represents C.sub.1-4 -alkyl.is hydrolyzed and subjected to an aldol condensation and, where R=C.sub.1-4 -alkoxy, the reaction product is subsequently subjected to an acid treatment.The compounds I are for the most part known flavoring substances.
Abstract: A process for the production of pimelic acid comprising reacting .epsilon.-caprolactone with carbon monoxide and water in the presence of a carbonylation catalyst, such as a Group VIII metal and hydrogen halide.
Type:
Grant
Filed:
October 9, 1984
Date of Patent:
December 19, 1989
Assignee:
National Distillers and Chemical Corporation