http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2001316385-A

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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D319-20
filingDate 2001-03-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2954ba262eb9ae16fb659dceb008f422
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6c3bff29ffc51c2dac828d52d5dcf6b1
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a93da2d148377490b5ac09cdeb332c67
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a6369f9f0175d0a5d789532dedd0f783
publicationDate 2001-11-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-2001316385-A
titleOfInvention Method for producing 1,4-benzodioxane derivative
abstract (57) Abstract: An industrial method for producing a 1,4-benzodioxane derivative. A catechol derivative represented by the following formula (2) and a glycidyl derivative represented by the following formula (3) are dissolved in an organic solvent. A method for producing a 1,4-benzodioxane derivative represented by the following formula (1), characterized by reacting in the presence of a fluorine salt. Embedded image (R 1 , R 2 and R 3 each represent a hydrogen atom, a halogen atom, A hydroxyl group, a nitro group, a cyano group, a formyl group, a hydroxycarbonyl group, an alkoxycarbonyloxy group, a saturated or unsaturated alkyl group, an amide group, etc., and X represents a halogen atom or a sulfonyloxy group. )
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2004011451-A1
priorityDate 2000-03-03-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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