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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_423ab0b422b79431d89cde80481a4821
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C275-54
filingDate 2006-08-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2009-12-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c7e13fc170f6ce673d903ed252f2c19f
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ba588220c41dd9dec60fc9ca4a8285b3
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2377083bc48af2fb138ca40973c9180a
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a6432b368664aecf3f26aa22021ccccd
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publicationDate 2009-12-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-100564355-C
titleOfInvention A kind of preparation method of benzoyl area kind derivative
abstract The present invention relates to a kind of preparation method of benzoyl area kind derivative, particularly substitute phosgene, trichloromethylchloroformate or oxalyl chloride directly and the chemical synthesis process of substituted aniline and substituted benzamide prepared in reaction benzoyl area kind derivative with two (trichloromethyl) carbonic ethers.In organic solvent,, obtain described benzoyl area kind derivative by the substituted benzamide shown in the substituted aniline shown in the formula (II) and two (trichloromethyl) carbonic ethers and the formula (III) in 20~200 ℃ of reaction 1~20h.That advantage of the present invention is is simple to operate, reactions steps is few, solvent loss is little, environmental friendliness, production safety is reliable, production cost is low, the reaction yield height, and toxicity is little, and corrodibility is little, has big industrialization potentiality and economic results in society.
priorityDate 2006-08-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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