http://rdf.ncbi.nlm.nih.gov/pubchem/patent/BR-0111039-A
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_4a8aeb1de632fe3cc89682e745ae0661 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ad90a59b73cc02665933b07864ed238b http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1e2c341dd2cda8fed16dbab95e3dae80 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5e4810c3a7ce1e91aa32126ebbea45ed |
| publicationDate | 2003-04-08-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | BR-0111039-A |
| titleOfInvention | Process for preparing 2-chloro-5-chloromethyl-1,3-thiazole |
| abstract | "PROCESS FOR PREPARATION OF 2-CHLOR-5-CHLOROMETIL-1,3-THIAZOL". Process for preparing 2-chloro-5-chloromethyl-1,3-thiazole, in which allyl isothiocyanate of the formula CH ~ 2 ~ = CH-CH ~ 2-NCS is reacted at -40 ° C to + 30 ° C <198> C in an inert solvent under reaction conditions with 1 to 2 moles of a chlorinating agent per mol of allyl isothiocyanate, the reaction mixture thus obtained is reacted at a reaction temperature of 0 <198> C to the boiling temperature of the solvent employed with 1 to 5 moles of oxidizing agent per mol of allyl isothiocyanate, whereby 2-chloro-5-chloromethyl-1,3-thiazole is isolated from the reaction mixture and optionally reacted. by crystallization to form highly pure 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.