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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_1d29f7ac2c7f9be9f7dae1a83bbb5c92
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D333-32
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D333-42
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D333-40
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D333-38
filingDate 1994-12-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2d1be3c68123447510df4c22fe78a1e2
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2cc3d9f9dd9f33f89ceb29546e481f70
publicationDate 1996-07-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-H08176141-A
titleOfInvention Method for producing thienyl ether derivative
abstract (57) [Summary] [Structure] The following general formula (1), (In the formula, R 1 represents a hydrogen atom, an alkoxycarbonyl group, etc., and R 2 represents a cyano group, an alkoxycarbonyl group, etc.), a basic alkali metal aqueous solution and a dialkyl sulfuric acid are hydrogen ions. The reaction is carried out in a concentration range of 6-11. [Effect] This is a production method in which water is basically used as a reaction solvent, and alkali sulfate of a by-product inorganic substance is dissolved in water. Therefore, the thienyl ether derivative can be obtained with good selectivity and high yield, without the need to perform the filtration operation of the by-product inorganic substance.
priorityDate 1994-12-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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