http://rdf.ncbi.nlm.nih.gov/pubchem/patent/SU-1336484-A1
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_ffb48902cf045bb30d646769fb5b56e6 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C211-00 |
| filingDate | 1985-12-30-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| grantDate | 1988-04-30-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_30fa7abd05b23fac457952e23f7003df http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_90e467a704d2c9c2a3c5b30b0a74b25a http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ffb40ce12321e9bed1290a581b5ca775 |
| publicationDate | 1988-04-30-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | SU-1336484-A1 |
| titleOfInvention | Method of producing n-monoalkyl-substituted o-nitroanilines |
| abstract | The invention relates to alkylated amines, and in particular to a method for producing N-mono-apyl substituted o-nit roanilines (MHA) of the general formula: lR / -3NO -4-NHRj-C4H, where a) with Rj-CHj or C, oHj, ; b) with or CHlO R, —CHj, amyl, hexyl, or deadl; c): with; R, j-CHj, amyl or decyl. Simplifying the process and increasing the yield of MNA is achieved by using other raw materials. Synthesis of MNA is carried out by alkylation of N-unsubstituted o-nitroaniline with the corresponding iodine alkyl in dimethyl sulfoxide or hexane tetapol with heating in the presence of potassium hydroxide. The method allows to increase the yield of MNA from 60 to 100% when carrying out the process in one stage without the introduction of activated amino groups. Od SAE (ZE 4; 00 m { |
| isCitedBy | http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-5189220-A http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-5210305-A |
| priorityDate | 1985-12-30-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 55.