Hydrochloric Acid → 3,3,3-Trifluoro-2-(trifluoromethyl)-1,2-propanediol
반응식
[OH:1][C:2]([C:11]([F:14])([F:13])[F:12])([C:7]([F:10])([F:9])[F:8])[C:3](OC)=[O:4].B.[Na].O.Cl>C(OCC)C>[F:8][C:7]([F:9])([F:10])[C:2]([C:11]([F:12])([F:14])[F:13])([OH:1])[CH2:3][OH:4]참가 물질
6
실험 절차
With stirring, 100 g of methyl 2-hydroxy-3,3,3-trifluoro-2-trifluoromethylpropionate was added dropwise to a mixture of 25.0 g sodium boron hydride, 500 g water and 500 g diethyl ether. Stirring continued for 10 hours, after which hydrochloric acid was added to quench the reaction. The organic layer was separated, concentrated, and distilled, obtaining 83.9 g of 3,3,3-trifluoro-2-trifluoromethyl-1,2-propane diol (yield 96%).
후처리
- stirringStirring
- customto quench
- customthe reaction
- customThe organic layer was separated
- concentrationconcentrated
- distillationdistilled
출처 및 근거
- ORD 기록
- ord-581c18f00d20498ebc21c1af0e00e8f8
- 출처 데이터셋
- uspto-grants-2009_02
- 특허 번호
- US07485408B2
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