http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-114292164-A

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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C33-42
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C29-86
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C29-44
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filingDate 2021-10-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_63c214155f085b7239d10e2977bd9311
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3844219a3d9d94ebb1311bd0ceeb3751
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_238297b0c94a000bb1e499ab04bd6661
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_302e3a9d3ba2badf458847f06a62ebd9
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_77245a9811c8f3486c052a348be628aa
publicationDate 2022-04-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-114292164-A
titleOfInvention Synthetic method of 4,4, 4-trifluoro-2-butenol
abstract The invention discloses a method for synthesizing 4,4, 4-trifluoro-2-butenol, which comprises the following steps: putting anhydrous methanol and an initiator into a reactor with illumination, replacing a system by N2, slowly introducing 1-X-3,3, 3-trifluoropropene under the illumination of light, and keeping the temperature until the reaction is complete after the introduction of the 1-X-3,3, 3-trifluoropropene; most of the methanol is evaporated under reduced pressure, and the concentrated solution is rectified to obtain 2-X-4,4, 4-trifluorobutanol; putting prepared 2-X-4,4, 4-trifluorobutanol into a reaction kettle, diluting with a solvent, adding a catalyst and a polymerization inhibitor, and adding alkali to remove HX; the 4,4, 4-trifluoro-2-butenol is obtained by layering, extraction, drying and concentration. The process has the advantages of low cost of raw materials, mild reaction conditions and high yield of over 80 percent.
priorityDate 2021-10-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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