http://rdf.ncbi.nlm.nih.gov/pubchem/patent/PL-358329-A1
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_173bc2c63b34988699010ba05e5b1376 |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D277-32 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D277-32 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D277-20 |
| filingDate | 2001-04-26-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1e2c341dd2cda8fed16dbab95e3dae80 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1d2d4d0838fe47d96de688aa97b5649e http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5e4810c3a7ce1e91aa32126ebbea45ed http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4a8aeb1de632fe3cc89682e745ae0661 |
| publicationDate | 2004-08-09-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | PL-358329-A1 |
| titleOfInvention | Production method for 2-chloro-5-chloromethyl-1,3-thiazole |
| abstract | A process for the preparation of 2-chloro-5-chloromethyl-1,3-thiazole, in which allyl isothiocyanate of formula CH2=CH-CH2-NCS is reacted at from -40° C. to +30° C., in a solvent that is inert under the reaction conditions, with from 1 to 2 mol of a chlorinating agent per mol of allyl isothiocyanate; to the reaction mixture so obtained there is added, at a reaction temperature of from 0° C. to the boiling temperature of the solvent used, from 1 to 5 mol of oxidising agent per mol of allyl isothiocyanate, and then 2-chloro-5-chloromethyl-1,3-thiazole is isolated from the reaction mixture and is optionally converted by crystallisation into high-purity 2-chloro-5-chloromethyl-1,3-thiazole. |
| priorityDate | 2000-05-23-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 19.