http://rdf.ncbi.nlm.nih.gov/pubchem/patent/HU-191343-B

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_38c4969f203ddc041ce0ce103c1bcfbf
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C33-34
filingDate 1982-03-03-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_edc40c872718ce765b74b8369c6bccb4
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_fb42ce088c02776a446f42f77c838557
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_177577cc346bd6777a80c809c8e3b50c
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4e3366fffd8de9d2a3f87ea5b52daa5b
publicationDate 1987-02-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber HU-191343-B
titleOfInvention Process for the hydroxy-methylation of nitro-phenil-alkanes
abstract FIELD OF THE INVENTION The present invention relates to the nitrophenyl alcohols of the formula (I): wherein the nitro group in the formula (I) is in the 2 or 4 position, X is hydrogen or halogen, C 1 -C 4 alkyl, C 1-4 alkoxy. - either nitro, R, hydrogen or C 1-4 alkyl, while R 2 is hydrogen or C 1-4 alkyl - Nitrophenyl alkanes of Formula II in Formula II are X, R, and R 2 refers to hydroxymethylation of dimethylformamide with a water content of 0.1 to 1% by weight of the above paraformaldehyde at 40-100%. According to the invention, the reaction is carried out in the presence of 2 to 6 mole% sodium or potassium cyanide catalyst and 5 to 20 mole% paraformaldehyde excess. CH1-OH (I) -1-
priorityDate 1982-03-03-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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