http://rdf.ncbi.nlm.nih.gov/pubchem/patent/SU-1712351-A1

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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C29-03
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C35-29
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C35-14
filingDate 1989-12-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1992-02-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_fbd665d371cfe9b46cc7afbd169ccc35
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_edba5ce81b3b1a22ee241cf7050e981e
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publicationDate 1992-02-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber SU-1712351-A1
titleOfInvention Method of cyclic diols synthesis
abstract The invention relates to cyclic dioles. in particular, the preparation of cyclic diols of a cyclohexane or bicycloheptane row of a common f-ly Rj-C (OH) -CR2COH) ~ n-Rj, -CH-CHj-GMRj-Ctt-tHi where n-R3 = -CHF? HGH2) 2-CH2 - or Ri, R2.R3 = H or CH3. stabilizers used in the manufacture of antioxidants. perfumes. The goal is to simplify the process, reducing the consumption of reagents and catalyst. For this purpose, hydroxylation of cycloolefinic hydrocarbons with hydrogen peroxide in the presence of molybdenum oxobromide and acetic acid is carried out at a molar ratio of 1 &lt; 1-1.1): [
priorityDate 1989-12-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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