http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-950029253-A
Outgoing Links
Predicate | Object |
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classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C235-16 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C231-12 |
classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C231-12 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/B01J31-02 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C233-66 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07B61-00 |
filingDate | 1994-04-07-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationDate | 1995-11-22-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber | KR-950029253-A |
titleOfInvention | Method for preparing 2 ', 3'-dichloro-4-ethoxymethoxybenzanilide |
abstract | The present invention aims to improve economics and improve yields by omitting the step of isolating 2 'and 3' dichloro-4-hydroxybenzanilide as a potassium salt and using a low-cost solvent. In the constitution, at least one polyalkylene polyol is added to the reaction mixture in the presence of an inorganic base, using an aromatic hydrocarbon as a solvent, and 2 ', 3'-dichloro-4-ethoxymethoxybenz In the preparation of the anilide, the step of isolating the raw material 2 ', 3'-dichloro-4-hydroxybenzanilide as a potassium salt can be omitted, and an expensive polar solvent such as N, N-dimethylformamide can be omitted. It is possible to use inexpensive aromatic hydrocarbons without the post-treatment loss after the completion of the reaction, and the economical efficiency can be remarkably improved, and the products 2 ', 3'-dichloro-4 Ethoxymethoxybenzanilide is characterized in that it has the effect of obtaining a good yield. |
priorityDate | 1994-04-07-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 27.