http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-S6144856-A

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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C233-91
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C231-00
filingDate 1984-08-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c517e3d846613381bd7f95fe719a4596
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d9cf92324d8b558f0f82909c3aecb85a
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_20e19a23d93797a30e78e49fc22079be
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_07fe0828676dfcfccfc200f851a3fe90
publicationDate 1986-03-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-S6144856-A
titleOfInvention Phenylacetaldehyde derivative
abstract NEW MATERIAL:The compound of formula I (X is halogen; R is lower alkyl). n EXAMPLE: 2-N,N-diacetylamino-6-acetoxy-3,5-dibromophenylacetaldehyde. n USE: A precursor of 4-hydroxyindole useful as a synthetic raw material of pharmaceuticals, dyes and agricultural chemicals. n PREPARATION: The compound of formula I can be prepared by the ozone oxidation and reduction of the novel compound of formula II. The compound of formula II is produced by acylating m-aminophenol with acid anhydride, etc., halogenating to the novel compound of formula III (R is other than methyl), reacting the compound of formula III with the allyl halide of formula IV (X' is halogen) to obtain the novel compound of formula V, and finally heating the compound in the presence of an acid anhydride having a boiling point of ≥170°C (e.g. caproic anhydride). n COPYRIGHT: (C)1986,JPO&Japio
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-103145570-A
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priorityDate 1984-08-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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