http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-S6034925-A

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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C67-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C45-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C45-29
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C47-565
filingDate 1983-08-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3d3006285650d9ed6329bb227806d41b
publicationDate 1985-02-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-S6034925-A
titleOfInvention Preparation of 2-hydroxyisophthalaldehydes
abstract PURPOSE: To obtain the titled substance useful as a raw material for a functional high polymer compound in high purity in high yield, by oxidizing a 2,6-bis(hydroxymethyl)phenol with MnO 2 . n CONSTITUTION: A compound shown by the formula I R is H, or 1W4C alkyl) is brought into contact with MnO 2 in a solvent such as chloroform, acetone, ether, etc. at about room temperature for several hours W several days, to give a compound shown by the formula II. Active MnO 2 obtained by thermal decomposition of manganese carbonate or manganese oxalate, or precipitation method from potassium permanganate and manganese sulfate, etc. is preferable as MnO 2 , and an amount of it used is 5W50 times as much as the compound shown by the formula I by weight. n EFFECT: After the reaction is over, the desired substance having practically sufficient purity is obtained simply by filtering the reaction solution to remove a Mn compound, followed by evaporating a solvent. n COPYRIGHT: (C)1985,JPO&Japio
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-8206748-B2
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priorityDate 1983-08-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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