http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-950029253-A

Outgoing Links

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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

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Total number of triples: 27.