http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-103232407-B

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_d86d2f4dd3ec8b041c390750a310f9a0
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D277-64
filingDate 2013-04-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2015-03-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f2a61733091e46ea85396cf68d2f8490
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_cce9feddd80e5ce6560a07ce949f387b
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_99d64391aaa9bd7b5fbebfe320bd35e7
publicationDate 2015-03-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-103232407-B
titleOfInvention Method for preparing 2-methylbenzothiazole derivative
abstract The invention discloses a method for preparing 2-methylbenzothiazole derivative with industrial application value, which comprises the following steps: adding acetic anhydride and 2-aminothiophenol halide into a glacial acetic acid reaction system, filtering after reaction; cooling the filtrate to 0-5 DEG C, slowly adding sodium hydroxide aqueous solution drop by drop, adjusting the system pH to pH=7.0+/-0.5; extracting by organic solvent, distilling and removing the organic solvent, obtaining the 2-methylbenzothiazole derivative. Compared with the prior art, the process provided by the invention has the advantages of simple operation without catalyst, low production cost, high efficiency, short reaction period and small dissipating energy, accordingly the invention can realize industrial scale production with repeatedly usable organic solvent and minimized environment pollution.
priorityDate 2013-04-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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