Predicate |
Object |
assignee |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_feb4980776635f9802e9003151ff0287 http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_39225fbb33f4b514bec75646a89fd794 http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_84912fe272d12502b43ac548d70b8bff http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_d669af06cb2abbcd6823699582a97002 http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_cf7e0f82720becafa8bd6ed018b516fd |
classificationCPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C253-30 |
classificationIPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C255-54 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C255-53 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C253-30 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C253-28 |
filingDate |
2003-09-04-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
inventor |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ee6105a6d1642296938fcd5bfafa8f00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_50411f49077ae699db3229a6c5cdd936 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c6e6c8de3f3f2a83e453afd35394ae65 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_dbf3949a7bdd6920769c0e208ac8be44 |
publicationDate |
2004-04-01-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber |
WO-2004026812-A2 |
titleOfInvention |
Method for catalyst-free production of cyanophenols from methoxybenzonitriles |
abstract |
According to the inventive method for catalyst-free production of cyanophenols from methoxybenzonitriles, substituted methoxybenzonitriles of general formula (I) are reacted with an alkali alcoholate at temperatures of 80 - 230 DEG C. The inventive method is based on simple, low-cost and easily accessible raw materials and can be carried out in technically simple conditions, enabling cyanophenols to be produced with high and partially quantitative yields with guaranteed low waste levels. Sodium methanolate is used as a preferred alkali alcoholate at preferred temperatures of 140 - 180 DEG C. The methoxybenzonitrile component can optionally be produced by ammonoxidation of a methoxytoluol of ammonia and (air-)oxygen and be directly further reacted. |
isCitedBy |
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2021212938-A1 |
priorityDate |
2002-09-11-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type |
http://data.epo.org/linked-data/def/patent/Publication |