http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CA-2512384-A1

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C43-123
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C29-10
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C43-12
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C29-124
filingDate 2004-01-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4d3433879e11c2b7bed237de053e8b75
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_213388f9dd7ec124d5f908a6e19a84c6
publicationDate 2004-08-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CA-2512384-A1
titleOfInvention Process for recovery of 1,1,1,3,3,3-hexafluoroisopropanol from the waste stream of sevoflurane synthesis
abstract Provided is a process of obtaining 1,1,1,3,3,3-hexafluoro-2-propanol ("HFIP") from a composition comprising an HFIP hydrolyzable precursor. The HFIP hydrolyzable precursor is a compound, other than sevoflurane itself, that has an intact 1,1,1,3,3,3-hexafluoroisopropoxy moiety[(CF3)2CHO~], and contains one or more moieties susceptible to acidic hydrolysis, such that HFIP is released upon such treatment. The process is useful, among other things, for recovering HFIP from waste streams associated with the synthesis of the inhalation anesthetic, fluoromethyl 2,2,2-trifluoro-1-(trifluoromethyl)ethyl ether ("sevoflurane"). The process includes heating the composition with a strong protic acid to a temperature effective to hydrolyze at least some of the HFIP hydrolyzable precursor to HFIP, and then isolating the HFIP from the heated composition.
priorityDate 2003-01-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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