http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2002302475-A
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_dbdfa36b677f4ef61245ca725011e221 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C249-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07B61-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C251-44 |
| filingDate | 2001-07-25-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_17ccd8c93e9459902074b0ad3e43d2c9 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5c3c1051b1f39438cc09c83c1721fcc3 |
| publicationDate | 2002-10-18-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | JP-2002302475-A |
| titleOfInvention | Method for producing cyclohexanone oxime |
| abstract | (57) [Problem] To provide a simple method for producing cyclohexanone oxime. SOLUTION: Using benzene as a starting material, partially hydrogenating cyclohexene, hydrating it to obtain cyclohexanol, aminating it to obtain cyclohexylamine, and partially oxidizing it to obtain cyclohexanone oxime, Are sequentially performed. [Effect] Cyclohexanone oxime can be produced by a simple method. That is, the number of reaction steps is small, In addition, the selectivity of each step is high, there is no need to use a reaction reagent produced in complicated steps such as hydroxylamine, and there is no by-product of ammonium sulfate. This is extremely advantageous for industrial implementation. |
| isCitedBy | http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-112939765-A http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-7408081-B2 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-112939765-B http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-111253281-A |
| priorityDate | 2001-01-31-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 107.