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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C213-08
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C255-59
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C217-84
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C215-76
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filingDate 1997-09-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 1998-07-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber KR-19980024647-A
titleOfInvention How to prepare aminophenol
abstract The present invention includes reacting a compound of Formula 3 or 4 with an organic halide of Formula 5 under aqueous acidic conditions, with periodic addition of an acid trapping agent so that there is no need to continuously monitor the pH of the reactants. It relates to a process for the preparation of N, N-unsubstituted aminophenols of the general formula (1) or (2).n n n Formula 1n n n n n n n n Formula 2n n n n n n n n Formula 3n n n n n n n n Formula 4n n n n n n n n Formula 5n n n R 2 Xn n n In the above formula,n n n R 1 and R 2 are the same or different and are each saturated or unsaturated aliphatic hydrocarbyl, cycloalkyl, aralkyl (the phenyl ring of aralkyl may be further substituted), alkoxyalkyl, or cycloalkylalkyl, provided that R 1 And R 2 is not methyl at the same time;n n n R 3 represents hydrogen or R 1 ;n n n R 'represents hydrogen, halogen, nitro, cyano, alkyl or alkoxy;n n n X represents a halogen.
priorityDate 1996-09-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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