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classificationIPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07B61-00
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C31-137
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C29-147
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C69-54
filingDate 2010-05-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_299f0c68120d21b8d7da573140e294da
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_55697c8c050a086e2932a15478267a4b
publicationDate 2011-12-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-2011246390-A
titleOfInvention Method for producing asymmetric tertiary alcohol
abstract An asymmetric tertiary alcohol having a cyclic skeleton is easily produced in a high yield. A method for producing an asymmetric tertiary alcohol includes a compound such as an acid halide having a cyclic skeleton represented by the following formula (2) R 1 -M 1 (2) [wherein R 1 represents a hydrocarbon group. Show. M 1 represents Li or the like, or —M a Y (wherein M a represents Mg or the like, Y represents a halogen atom), and then reacted with the following formula (3 ) R 2 -M 2 (3) [wherein R 2 represents a hydrocarbon group. However, R 1 and R 2 are different groups. M 2 is Li or the like, or -M b Y (wherein M b is Mg, Y represents a halogen atom) is reacted with an organometallic compound represented by the following formula (4) [Wherein, ring Z represents a non-aromatic or aromatic ring], and is characterized by obtaining an asymmetric tertiary alcohol. [Selection figure] None
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priorityDate 2010-05-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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