http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-102796003-B

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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C205-12
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C201-08
filingDate 2012-07-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2014-05-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_923d8b037a817dfa0f5d1f0933d9fa20
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_89e72928ecbe571d332030909cc14c2a
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_0262e061f2c6e1ef705eec225c659e97
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_cf4952edc83adeb1892102fbc74cd137
publicationDate 2014-05-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-102796003-B
titleOfInvention Preparation method of 2-fluoro-4,5-dichloronitrobenzene
abstract The invention discloses a preparation method of 2-fluoro-4,5-dichloronitrobenzene, relating to the technical field of preparation of medicine and pesticide intermediates. The industrialized preparation method of the 2-fluoro-4,5-dichloronitrobenzene comprises the following steps: by using 4-fluoroaniline as an initial raw material, carrying out acetylation, chlorination, hydrolysis, diazotization-Sandmeyer reaction and nitrification to synthesize the 2-fluoro-4,5-dichloronitrobenzene. The 2-fluoro-4,5-dichloronitrobenzene prepared by the method disclosed by the invention is a light yellow solid, and the purity is 98.5%; the raw material conversion rate for each reaction step reaches 100%; and the total yield of the whole process is up to 27.1%.
priorityDate 2012-07-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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