http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-H0840986-A
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_6831b19bfc354357342f7c7da79fc162 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C68-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C69-96 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07B61-00 |
| filingDate | 1994-07-28-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5aed4d7a31e1ba5c27726ced8e3eed4c http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d3a9a7229953746cff4a8d8ee85561ad http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e3147872d242c1373e5fe2c8f441391b |
| publicationDate | 1996-02-13-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | JP-H0840986-A |
| titleOfInvention | Manufacturing method of monochloromethyl chloroformate |
| abstract | (57) [Summary] [Structure] Methyl chloroformate is reacted with sulfuryl chloride, and the obtained monochloromethyl chloroformate is represented by the general formula [II] ROH [II] (wherein R is a linear or branched lower alkyl group). Group, a cycloalkyl group or a phenyl group) is reacted with an alcohol compound represented by the general formula [I] RO-COOCH 2 Cl [I] (wherein the symbols have the same meanings as described above). A method for producing an alkoxycarbonyloxymethyl chloride compound represented by the formula (1). [Effect] Methyl chloroformate can be selectively monochlorinated without using chlorine gas, whereby an alkoxycarbonyloxymethyl chloride compound can be obtained safely and in high purity. |
| isCitedBy | http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2012532910-A http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-103965044-A |
| priorityDate | 1994-07-28-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 46.