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6977315 |
Process for producing optically active nitroalcohols
The present invention relates to a process for producing optically active β-nitroalcohols wherein nitroaldol reactions of aldehydes and nitroalkanes are carried out in the presence of a base and...
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6358431 |
Calixarenes
A method of imparting a water repellent surface to a hydrophilic substrate which comprises contacting the substrate with a solution or dispersion of a suitable calixarene in a liquid medium.
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6265621 |
Process for producing halogenated phenol compounds
The present invention provides a process for producing a halogenated phenol compound represented by the general formula [II]: ##STR1## wherein Q is a monovalent organic residue, A is, the same or...
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5847231 |
Selective nitration of phenol derivatives
Process for preparing 4-nitrophenol derivatives of formula (IV) with high selectivity, which comprises converting phenols to diphenyl oxalate derivatives of formula (III) and conducting nitration...
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5817888 |
Bromination process
A bromination process for organic compounds employs stabilized bromine chloride solutions as the brominating agent. Activated aromatic compounds such as anisole can be selectively monobrominated in...
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5773651 |
Process for the preparation of fluorine-containing chemical compounds
Process for the preparation of fluorine-containing compounds by reduction in a container provided with a stirrer, the stirrer being constructed entirely or partly of a carbon material.
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5414148 |
Preparation of p-nitrophenolic compounds
p-Nitrophenolic compounds, e.g., p-nitrophenol itself, are selectively prepared by (a) reacting a phenolic compound with a nitrosating agent in the presence of sulfuric acid, the concentration of...
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5393776 |
Tocotrienol analogs in the treatment of hypercholesterolemia and hyperlipidemia
This invention relates to structurally novel acyclic tocotrienol analogs, which are useful for cholesterol/lipid lowering in cases of hypercholesterolemia and hyperlipidemia, and for...
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5371291 |
Synthesis of 4,6-diaminoresorcinol
The invention is a new process for preparing 4,6-diaminoresorcinol, a precursor to polybisbenzoxazoles. The desired product is prepared from resorcinol by incorporating a halo group on the...
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RE34745 |
High purity process for the preparation of 4,6-diamino-1,3-benzenediol
High purity 4,6-dinitro-1,3-benzenediol is prepared by (a) contacting a 1,2,3-trihalobenzene with a nitrating agent and an acid under reaction conditions such that a...
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RE34589 |
Aqueous synthesis of 2-halo-4,6-dinitroresorcinol and 4,6-diaminoresorcinol
The displacement of halogen from a 1,2,3-trihalo-4,6-dinitroresorcinol can be carried out in an aqueous medium using alkali metal hydroxide to form 2-halo-4,6-dinitroresorcinol. The product is a...
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5292967 |
Process for producing 2,3-difluoro-6-nitrophenol
According to a process for producing isomer-free 2,3-difluoro-6-nitrophenol, 2,3,4-trifluoronitrobenzene is reacted with an aqueous solution of alkali metal or alkaline earth metal hydroxide in the...
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5292932 |
Process for the preparation of 5-chloro-2-hydroxy-4-alkyl-benzenesulfonic acids
Process for the preparation of compounds of the formula (1) ##STR1## in which R is an alkyl (C 1 -C 6 ) group and X is a hydrogen or alkali metal atom, in which compounds of the formula (2)...
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5292966 |
Process for the preparation of 2-nitro-3, 6-dichlorophenol
2-Nitro-3,6-dichlorophenol is prepared by sulfonation of 2,5-dichlorophenol and subsequent nitration and desulfonation, in which the nitration is carried out by metering in a nitrating acid...
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5227535 |
Process for the preparation of 2-nitro-5-fluoro- or -5-chlorophenol
The present invention relates to a process for the preparation of isomerically pure 2-nitro-5-fluoro- or -5-chlorophenol, by reacting 2,4-difluoronitrobenzene or 2,4-dichloronitrobenzene with...
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5204242 |
Substituted phenols
The present invention provides a colorimetric process for the detection of an oxidative coupling reaction in which a coupling component is reacted with a developer component in the presence of an...
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5136109 |
Process for preparing 2,4-dichloro-3-alkyl-6-nitrophenols
2-4-Dichloro-3-alkyl-6-nitrophenols which are useful as intermediate of cyan couplers in color photography are prepared by sulfonating 4-chloro-3-alkyl-phenols to obtain...
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5012015 |
Process for producing 2,4-dichloro-3-alkyl-6-nitrophenol
2,4-Dichloro-3-alkyl-6-nitrophenol, which is a precursor of 2,4-dichloro-3-alkyl-6-aminophenol useful for the production of a cyan coupler to be used with a sensitive material in the field of a...
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4978808 |
Method of producing 2,2-bis(3-nitro-4-hydroxyphenyl)hexafluoropropane
Disclosed herein is a method of producing 2,2-bis(3-nitro-4-hydroxphenyl)hexafluoropropane, which comprises (a) preparing 2,2-bis(4-hydroxyphenyl)hexafluoropropane and a lower fatty acid; and (b)...
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4962198 |
Process for the hydroxylation of electrophilic aromatic compounds
The invention relates to a generally applicable process for the hydroxylation of electrophilic aromatic compounds, according to which the electrophilic aromatic compounds are reacted with organic...
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4960955 |
Process for making 4-chloro-2-methyl-5-nitro-phenol
The process of making 4-chloro-2-methyl-5-nitro phenol (I) ##STR1## comprises nitrating a 4-chloro-2-methyl-phenyl sulfonate of the formula (II) at the 5 position ##STR2## in which R is a residue...
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4954662 |
Selective chlorination of ortho-substituted phenols
Ortho-substituted phenolic compounds, e.g., 2,6-dichlorophenol, are selectively chlorinated, e.g., into 2,4,6-trichlorophenol, with gaseous chlorine in either the molten state or in a solvent...
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4943666 |
Process for producing nitrophenol compound
An improved industrial process for producing a compound of the general formula: ##STR1## wherein R is an alkyl group having 1 to 4 carbon atoms which comprises reacting a compound of the general...
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4885388 |
2-methyl-4-fluoro-phenols and their preparation
New 2-methyl-4-fluoro-phenols and process for their preparation from 2-methyl-4-fluoro-phenol.
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4879415 |
Process for the preparation of chloronitroanilines and chloronitrophenols
The invention relates to a process for the preparation of chloronitroanilines or chloronitrophenols, which comprises chlorinating nitroanilines or nitrophenols in hydrochloric acid by adding...
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4827047 |
Chlorination of nitrophenols
The chloronitrophenols, e.g., 2,6-dichloro-4-nitrophenol (a known agrochemical/pharmaceutical intermediate), are efficiently prepared by chlorinating ortho- or para-nitrophenol with gaseous...
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4723043 |
Nitration of phenolic compounds
Substituted phenols are nitrated by contacting same with a 10 to 70% by weight concentrated aqueous solution of nitric acid. The subject nitration process is well adopted for the preparation, e.g.,...
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4720595 |
Novel agents containing the compound 3-trifluoromethyl-4-nitrophenol
Agents which contain a combination product of 30 to 90% by weight of 3-trifluoromethyl-4-nitrophenol, which contains 12 to 20% by weight of water, with 10 to 70% by weight of a basic salt of the...
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4670608 |
Preparation of 2,4-dichloro-3-alkyl-6-nitrophenols
2,4-Dichloro-3-alkyl-6-nitrophenols are prepared by chlorinating, with chlorine in the presence of a catalyst, 1-alkyl-4-nitrobenzenes having a C 2 -C 8 -alkyl radical until the content of...
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4596893 |
2-trifluoromethyl-4,6-dinitro-phenol and derivatives thereof, process for the preparation thereof and herbicidal, acaricidal and crop regulation compositions containing same
The present invention relates to 2-trifluoro-methyl-4,6-dinitro-phenol and derivatives thereof prepared by hydrolyzing 2-chloro-3,5-dinitrobenzotrifluoride with an alkali hydroxide or alkaline...
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4581178 |
Addition of aldehydes to organic compounds having a carbon-hydrogen bond activated by a nitro or nitrile group
Low valent transition metal complexes containing small cone angle phosphine or arsine ligands efficiently catalyze addition of aldehydes to compounds or groups having a C--H bond activated by a...
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4558040 |
Miticidal (2-alkyl-3,4-dihydro-2H-1-benzopyran-8-yl)-diazenecarboxylic acid esters
Certain miticidal (2-alkyl-3,4-dihydro-2H-1-benzopyran-8-yl)diazenecarboxylic acid esters.
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4551264 |
Polyhalogenoaromatic compounds for liquid crystal compositions
New polyhalogenoaromatic compounds of Formula I ##STR1## wherein Y and Z are each independently alkyl, alkoxy or alkanoyl each of 1 to 12 C atoms, --COOR 1 , --O--CO--R 1 , CN, NO 2 , NH 2 or OH; ...
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4540832 |
Process for the preparation of 6-chloro-2,4-dinitrophenol
A process for the preparation of 6-chloro-2,4-dinitrophenol in a high yield and in a high degree of purity by saponifying 2,4-dinitrochlorobenzene and/or 2,4-dinitrophenyl alkyl ethers of the...
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4473713 |
Hydrolysis of aryl-aliphatic ethers
At least one of the other functions comprising an aryl-aliphatic ether, e.g., veratrol, is catalytically hydrolyzed with water, e.g., to guaiacol, in the presence of a catalytically effective...
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4347148 |
Full and lubricant compositions containing nitro phenols
Nitro phenols of the general formula ##STR1## wherein R is an aliphatic substituent of at least about 40 carbon atoms, a, b and c are, for example, each 1, 2 or 3, and Ar is an aromatic moiety such...
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4310711 |
Process for preparing 5-chloro-2-nitrophenol
A process for preparing 5-chloro-2-nitrophenol from 2,4-dichloronitrobenzene and excess alkali metal hydroxide in the presence of aprotic polar solvents at 20° to 150° C.
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4310702 |
Selective monochlorination of ketones and aromatic alcohols
Sulfuryl chloride is reacted in the liquid phase with an organic reactant which is a ketone or aromatic alcohol unsubstituted on both ortho carbons in the presence of a moderator selected from the...
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4283565 |
Process for preparing benzylalcohols
There is described an essentially two step process for the preparation of benzylalcohols including those benzylalcohols having substituents on the benzyene ring by reaction of a substituted or...
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4224244 |
9-Phenyl 5,6-dimethyl-nona-2,4,6,8 tetraenal or tetraenol derivatives
Novel 9-phenyl 5,6-dimethyl-nona-2,4,6,8-tetraenoic acid, tetraenal or tetraenol derivatives useful as anti-tumor agents.
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4120863 |
Fluorine-containing benzoxazoles
Benzoxazoles substituted in the 2-position with a perfluoroalkylether radical and bis-benzoxazoles in which the 2-position carbon atoms of the benzoxazole rings are attached to one another with a...
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4069340 |
Immonium salts and derivatives thereof
There are provided: novel aryloxy immonium salts, prepared by the reaction of their corresponding haloformates with amides; and phenolic compositions corresponding to the aryloxy immonium salts....
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4057419 |
2,4-Bis-(trifluoromethyl)-6-nitrophenol compounds and herbicidal compositions
Novel 2,4-bis-(trifluoromethyl)-6-nitrophenol compounds of the formula ##STR1## in which X is hydrogen; M; HNR.spsp.+ 1 R 2 R 3 ; --COR 4 ; --COOR 5 ; N,N-dimethylaminocarbonyl; --SO 2 R 6 ...
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4038328 |
Process for preparing 2-nitro-4,6-dichloro-5-methylphenol
2-NITRO-4,6-DICHLORO-5-METHYLPHENOL IS PREPARED BY THE SULFONATION OF 4-CHLORO-5-METHYLPHENOL TO FORM 2-SULFO-4-CHLORO-5-METHYLPHENOL WHICH IS CHLORINATED TO 2-SULFO-4,6-DICHLORO-5-METHYLPHENOL...
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4031249 |
Compositions containing certain 2,4-halo-6-nitrophenols or derivatives thereof and methods for using same to eradicate internal parasites in warm-blooded animals
A composition of matter for treating warm-blooded animals to eradicate internal parasites comprising a compound chosen from the group consisting of 2,4-dibromo-6-nitrophenol ...
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3985761 |
Nitrothiazolyl derivatives of nitrostyrene
Hydroxy substituted nitrostyrene derivatives have been found to exhibit antibacterial and anthelmintic properties. Derivatives having a nitrothiazolyloxy moiety have low toxicity and a broad...
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3954936 |
O-nitrosophenols as extractants for metal values
O-Nitrosophenols adapted for the liquid-liquid extraction of metals, e.g., copper, from aqueous solutions and a nitrosation process for the preparation of the phenols.
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3936447 |
7-Acylamino-desacetoxy-cephalosporanic acid esters and their production
7-Acylamino-desacetoxy-cephalosporanic acid esters are produced by heating a sulfoxide of 6-acylaminopenicillanic acid ester at a temperature of from about 60°C to about 150°C in the presence of...
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3929907 |
Halogenation of phenolic compounds
Aromatic and heterocyclic compounds are halogenated by a combination of chlorine, bromine or iodine and hydrogen peroxide, preferably in a two-phase system containing water and an organic liquid.
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3928470 |
Preparation of 2-nitrohalophenols
The polyhalonitrobenzenes bearing but a single halogen atom at either, but not both, of those molecular sites ortho to the nitro substituent thereof, are dehalohydroxylated to form their...
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