http://rdf.ncbi.nlm.nih.gov/pubchem/patent/SU-1456406-A1
Outgoing Links
Predicate | Object |
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assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_dcfd1c3317d2aa8325ee7c08a834e1a4 http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_1c0ce3574fac2bf5502b03fbfb6788bf |
classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C225-22 |
filingDate | 1987-03-19-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
grantDate | 1989-02-07-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_10d04c1022e80abc4c45ce50482e1302 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_756e1c925aeeba3f8c340302304a2c1f http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2d054eeae68120b1b749025141e5b4f2 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1bf018085dd9ddb7b63b8c69f8d551e6 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4dbce09fa0dcb8a0a4daf6ffe795d30e http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_eb725fdb1820e4da2479759df34207a8 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_92ec1cfed7da22128e3a95933198f55b http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_43c2c14a8e36780ededfce8bd01c97a0 |
publicationDate | 1989-02-07-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber | SU-1456406-A1 |
titleOfInvention | Method of producing 2-aminobenzophenone or its 2ъ-derivatives |
abstract | The invention relates to alpha amines, in particular the preparation of 2-adenobenzophenone or its 2-methyl- or 2-methoxy-substituted intermediates for the synthesis of chiral reagents used in the production of d-amino acids. The goal is to increase the yield of the target product and simplify the process. The latter is derived from the phenylmagnesium Bromide derivative and 2-methyl-3,1, 4-benzoxaz-4-one in the medium and ether mainly at. (-40) - (+10) C and subsequently separating the magnesium and solvent salts from 2- acetamide derivative, its hydrolysis of conc. HCl when heated, alkalinized to isolate the desired product. The starting 2-methyl-3, 1,4-benzoxaz-4-one is used in the form of a 1.5-2 M solution in CH, C1 2. The reaction products, after removing the solvent, are directly dissolved in an aqueous solution of HCl. These conditions allow the yield of the target product from 30 to 68-73% while reducing the number of operations using smaller volumes of solvent. 1 hp f-ly, 1 tab. $ W |
priorityDate | 1987-03-19-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 35.