http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2006182740-A
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_f9ba304908c7187b486482f16a0f6158 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D301-26 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D303-16 |
| filingDate | 2004-12-28-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_645cfbf9e26f97d7df052b0f34fc9ed5 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5c8a5be63a4420dfc1078fbee0da1a4c http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_07ec57d81ba43ea69cfc1c1611dd189d |
| publicationDate | 2006-07-13-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | JP-2006182740-A |
| titleOfInvention | Method for producing glycidyl sulfonate derivative |
| abstract | The present invention provides a simple and high-yield production method of a glycidyl sulfonate derivative useful as a synthetic intermediate for pharmaceuticals, agricultural chemicals and physiologically active substances. When a 3-chloro-1,2-propanediol derivative is used as a starting material, a glycidol derivative is obtained as an intermediate, and then a glycidyl sulfonate derivative is synthesized, the first step is 3-chloro-1,2 The reaction of the propanediol derivative is carried out in the presence of an organic solvent in the presence of an alkali metal or alkaline earth metal hydroxide. [Selection figure] None |
| isCitedBy | http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-114479053-A |
| priorityDate | 2004-12-28-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 88.