Abstract:
The disclosure is directed to: (a) phosphacycle ligands; (b) catalyst compositions comprising phosphacycle ligands; and (c) methods of using such phosphacycle ligands and catalyst compositions in bond forming reactions.
Abstract:
Provided is a gem-dinitro ester compound, represented by Formula 1 below: wherein R is a substituted or unsubstituted straight-chain or side-chain alkyl group of C2˜C12.
Abstract:
A method for producing a β-nitrostyrene compound is provided in which a benzaldehyde derivative represented by the following formula (I): and nitromethane are condensed in an acetic acid solvent in the presence of a primary amine. This method allows production of a β-nitrostyrene compound at a high yield in the industrially-safe reaction temperature range.
Abstract:
There are provided 4-Hydroxy-2'-nitrobutyrophenone and tetrahydro-2-(o-nitrophenyl)-2-furanol and mixtures thereof, important intermediates in the preparation of the crop-selective herbicidal agent 1-{[o-(cyclopropylcarbonyl)phenyl]sulfamoyl}-3-(4,6-dimethoxy-2-pyrimidinyl)urea. Also provided is a method for the preparation of 4-halo-2'-nitrobutyrophenone, useful as an intermediate in the preparation of 1-{[o-(cyclopropylcarbonyl)phenyl]sulfamoyl}-3-(4,6-dimethoxy-2-pyrimidinyl)urea.
Abstract:
Disclosed is a process for producing pentachloronitrobenzene (PCNB) by the reaction of pentachlorothiophenol with nitric acid in the presence of sulfuric acid or oleum.
Abstract:
A process of making nitroalkanes which comprises reacting a lower alkanol, e.g. methanol, and nitric acid (HNO.sub.3) in the vapor phase in the presence of a catalyst which is an oxide or a salt of a metal of Group II of the periodic table, e.g. calcium chloride.
Abstract:
The disclosure is directed to: (a) phosphacycle ligands; (b) catalyst compositions comprising phosphacycle ligands; and (c) methods of using such phosphacycle ligands and catalyst compositions in bond forming reactions.
Abstract:
A method for synthesizing 3,5-dichloroanisole from 1,3,5-trichloro-benzene is proved. The method may comprises: a) the reaction between 1,3,5-trichloro-benzene and a methanolate of an alkaline or alkaline-earth metal in a first solvent chosen from among dimethylsulfoxide and 1,1,3,3-tétramethylurea, b) the precipitation of the product resulting from step a) in a second solvent which is not included among substances considered carcinogenic, mutagenic and/or toxic for reproduction by Regulation (EC) no 1272/2008 of the European Parliament and of the Council of 16 Dec. 2008, then c) the recovery of the precipitate thus obtained. The method may be applied to synthesize 1,3,5-triamino-2,4,6-trinitrobenzene in which 3,5-dichloroanisole is an intermediate product.
Abstract:
Aromatic amines are produced by catalytic hydrogenation of corresponding aromatic nitro compounds in the gas phase, by carrying out the hydrogenation in the presence of catalysts which, besides palladium, vanadium and lead, contain in addition molybdenum, tungsten and/or rhenium on a ceramic support having a BET surface area of less than 40 m.sup.3 /g, at temperatures of from 180.degree. C. to 500.degree. C. in a catalyst bed and in a molar ratio of hydrogen to the nitro group or nitro groups of 3:1 to 30:1.