专利号:US-4578514-A 优先权日:1984-11-01 标题 :Synthesis of sulfilimines 发明人:GETMAN DANIEL P 权利人:MONSANTO CO 摘要:Processes are disclosed for preparation of N-aryl-S,S-dihydrocarbylsulfilimines by reaction of phenylisocyanate compounds with hydrocarbyl sulfoxides. The sulfilimines can be rearranged to ortho-thioalkylene anilines and the reactions can be employed in a route for converting nitrobenzene compounds to ortho-thioalkylene anilines, which are useful intermediates for preparation of herbicidal compounds.
专利号:EP-0197706-B1 优先权日:1985-04-01 标 题 :Synthesis of bromethalin intermediate 摘要:The present invention provides a process for preparing N-methyl-2,4-dinitro-N-phenyl-6-(trifluoromethyl)-benzenamine comprising treating 2-chloro-3,5-dinitrobenzotrifluoride in the presence of N,N-dimethylformamide and pyridine with a fluorinating reagent to provide 2-fluoro-3,5-dinitrobenzotrifluoride, which is finally reacted with N-methylaniline.
专利号:US-4476315-A 优先权日:1982-04-30 标 题:Nucleophilic substitution process 发明人:STAHLY G PATRICK; STAHLY BARBARA C 权利人:ETHYL CORP 摘要:Nitroarylacetic acid esters are prepared by reacting a nitroaromatic compound which is devoid of halogen on the aromatic ring carrying a nitro group with an alpha,alpha-disubstituted acetic acid ester in an inert solvent and in the presence of a base so that the ester undergoes a nucleophilic substitution on an unsubstituted ring carbon of the nitroaromatic compound during which an alpha-substituent functions as a leaving group. Nitrobenzene acetic acids and their esters are useful intermediates for the synthesis of pharmaceuticals.
专利号:RU-2118637-C1 优先权日:1997-03-25 标题:Method of synthesis of 10-(2,3,4-trimethoxy-6-methylphenyl)-decanoic acid ethyl ester
专利号:WO-8810247-A1 优先权日:1987-06-19 标题:Novel synthesis of 3-amino-2-methylbenzotrifluoride
专利号:US-4668830-A 优先权日:1984-12-26 标 题 :Process for the preparation of compounds containing a difluoromethylene or trifluoromethyl group 发明人:DESBOIS MICHEL 权利人:RHONE POULENC SPEC CHIM 摘要:A process for the preparation of compounds containing a difluoromethylene or trifluoromethyl group. A compound containing a carbonyl group, preferbly an acid, acid halide, amide, ketone or any compound containing a perhaloalkylcarbonyl moiety is placed, in anhydrous liquid hydrofluoric acid, in contact with boron trifluoride in a quantity such that the absolute pressure of boron trifluoride in the reaction system is at least one bar for a time sufficient to convert the carbonyl group to a difluormethylene or trifluoromethyl group. n The compounds obtained are useful as synthesis intermediates in the pharmaceutical, plant-protection and dye industries, as anesthetics or as heat-transfer and lubricating fluids.
摘要:Weast, R.C. and M.J. Astle. CRC Handbook of Data on Organic Compounds. Volumes I and II. Boca Raton, FL: CRC Press Inc. 1985., p. V1 263 摘要:SRI 摘要:2024 Emergency Response Guidebook, 摘要:National Toxicology Program, Institute of Environmental Health Sciences, National Institutes of Health (NTP). 1992. National Toxicology Program Chemical Repository Database. Research Triangle Park, North Carolina. 摘要:Il'chenko, A. Y., Science of Synthesis, (2005) 18, 1142.