http://rdf.ncbi.nlm.nih.gov/pubchem/patent/GB-1123539-A
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_e406a1a6e2d7dc346296914fdd695b58 |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C309-00 |
| filingDate | 1967-07-31-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5d4007c701d9d313e24db572f329cfb4 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_baff838c6d7f2a48eb8a1f0589447a1a http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_84f69d791996d5b553d7293d11b5255e |
| publicationDate | 1968-08-14-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | GB-1123539-A |
| titleOfInvention | Process for the production of n-substituted ammonium allyl- and methallyl-sulphonates |
| abstract | N-substituted ammonium allyl and methallyl sulphonates are prepared by reacting an allyl- or methallyl-halide with a metal sulphite to yield a mixture of a metal alkenyl sulphonate and a metal halide which is treated with an aqueous solution of an amine hydrochloride at pH 1-8. The amine hydrochloride may be provided in a solid form, in aqueous solution or it may be formed in situ from equivalent amounts of conc. HCl and the amine. The preferred amines are C2- 7 primary-, C2- 8 secondary - and C3- 14 tertiary amines or an amine which contains the N atom as a hetero atom in a ring system. In the examples allyl chloride and sodium sulphite yield sodium allyl sulphonate and NaCl and the reaction product is then treated with (1) and (2) n-butylamine hydrochloride and (3) dimethylamine hydrochloride. |
| isCitedBy | http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-108675947-A http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-108675947-B |
| priorityDate | 1967-07-31-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 31.