Water → 1-Octen-3-yl 2,3,3,3-tetrafluoropropionate

HRID 893816노트

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HRID 893816 반응식
[CH2:1]=[CH:2][C@H:3]([OH:9])[CH2:4][CH2:5][CH2:6][CH2:7][CH3:8].N1C=CC=CC=1.[F:16][CH:17]([C:21]([F:24])([F:23])[F:22])[C:18](Cl)=[O:19].O>ClCCl>[F:16][CH:17]([C:21]([F:24])([F:23])[F:22])[C:18]([O:9][CH:3]([CH2:4][CH2:5][CH2:6][CH2:7][CH3:8])[CH:2]=[CH2:1])=[O:19]

참가 물질

6

실험 절차

In 200 ml of dichloromethane were dissolved 28 g (0.22 mol) of (R)-(-)-1-octen-3-ol (92%ee) and 21 ml (0.26 mol) of pyridine, and then 39.5 g (0.24 mol) of 2,3,3,3-tetrafluoropropionyl chloride was dropwise added to the above-obtained solution while the solution was being cooled with ice. The resulting mixture was stirred at room temperature for 1 hour, subsequently water was added thereto, and then the reaction mixture was subjected to extraction with ether. The resulting extract was washed with 1N hydrochloric acid, a 5% aqueous solution of sodium hydrogencarbonate, and brine, and then dried with magnesium sulfate. Subsequently, the solvent was removed under reduced pressure, and the residual product was distilled at 95° C. under 25 mmHg, thereby obtaining 42.3 g of 1-octen-3-yl 2,3,3,3-tetrafluoropropionate in a yield of 76%.

후처리

  1. temperaturewas being cooled with ice
  2. extractionthe reaction mixture was subjected to extraction with ether
  3. extractionThe resulting extract
  4. washwas washed with 1N hydrochloric acid
  5. dry with materiala 5% aqueous solution of sodium hydrogencarbonate, and brine, and then dried with magnesium sulfate
  6. customSubsequently, the solvent was removed under reduced pressure
  7. distillationthe residual product was distilled at 95° C. under 25 mmHg

출처 및 근거

ORD 기록
ord-575bf172db914618a3549ec067517f6c
출처 데이터셋
uspto-grants-1992_06
특허 번호
US05126482

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