http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-102936192-B

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_303048b00b00faa67a9a510f988cdb52
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C49-747
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C45-45
filingDate 2012-11-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2015-01-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_0df04faa9abef638e18bc30d469a8731
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e05d8820ac4a1263bb23d8db1c7a3533
publicationDate 2015-01-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-102936192-B
titleOfInvention Method for synthesizing acetyl dithranol
abstract The invention discloses a method for synthesizing acetyl dithranol. The method comprises steps of dissolving anthralin in toluol, adding pyridine when the solution is cooled to the temperature from -5 DEG C to 4 DEG C, adding acetyl chloride after even stirring, conducting the reaction for 30-40 minutes at the temperature from -3 DEG C to 8 DEG C, and obtaining a solution containing the acetyl dithranol. The mol ratio of the acetyl chloride and the anthralin is 12.4-14.0, the use amount ratio of the anthralin and the toluol is 1g: 34-42ml, and the use amount mol ratio of the pyridine and the toluol is 12.0-14.0. Based on a prior method, the solvent is replaced, the reaction condition is optimized, the modified process line is improved, the reagent toxicity is reduced, the cost is reduced and the yield is improved compared with the yield reported by foreign documents.
priorityDate 2012-11-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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