http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-102516047-B

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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C47-55
filingDate 2011-12-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2013-11-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_0357c98e975316d082343fbc2dab70bf
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e010bee5358b796904ba0237596f06bb
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publicationDate 2013-11-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-102516047-B
titleOfInvention Preparation methods of 2-(trifluoromethyl)benzaldehyde and intermediate thereof
abstract The invention discloses a preparation method of 2-(trifluoromethyl)benzaldehyde, which comprises the following step: under the action of C1-C4 linear chain saturated monobasic fatty acid and C1-C4 linear chain saturated monobasic fatty acid salt of alkali metal, hydrolyzing 2-(trifluoromethyl)dichlorotoluene with water at a temperature of 150-190 DEG C and under a pressure of 0.3-0.78MPa. The invention also discloses a preparation method of an intermediate of 2-(trifluoromethyl)benzaldehyde, which comprises the following steps: performing selective fluoridation of 2-(trifluoromethyl)dichlorotoluene and hydrogen fluoride under the catalysis of antimony halidesantimony halides, wherein the molar concentration is 2-6 times of that of 2-(trifluoromethyl)dichlorotoluene, and the temperature of selective fluoridation is 60-110 DEG C. The preparation methods disclosed by the invention is simple in operation, low in cost, environment-friendly, and high in yield and purity, and can be better applicable for industrial production.
priorityDate 2011-12-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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