http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-H02268149-A
Outgoing Links
Predicate | Object |
---|---|
assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_03d0f52bb4069f8a19d70dcfb697c67a |
classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C309-75 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C309-73 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C303-28 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/B01J27-232 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/B01J23-04 |
filingDate | 1989-04-07-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3b4e36cd8db18de1dbe3dc7a249a8852 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b7aa5fb0d0d895d383fd8f151ca9d731 |
publicationDate | 1990-11-01-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber | JP-H02268149-A |
titleOfInvention | Toluenesolfonate |
abstract | NEW MATERIAL:A 2-methyl-2-β-aryloxyethyl-p-toluenesulfonate. n EXAMPLE: 2-Methyl-2-β-phenoxyethyl-p-toluenesulfonate. n USE: A medicine, agricultural chemical, raw material for recording materials and additrive. n PREPARATION: A 2-methyl-2-β-aryloxyethanol is reacted with p-toluenesulfonyl chloride in a solvent, such as acetonitrile, at -10 to +130°C using a base (e.g. caustic soda) as a catalyst. The 2-methyl-2-β-aryloxyethanol is obtained by reacting phenols with propylene oxide, reductively reacting an α-methyl-α- aryloxyacetic acid ester, etc. n COPYRIGHT: (C)1990,JPO&Japio |
priorityDate | 1989-04-07-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 28.