Diketene → HCID 86758741, 화합물

HRID 2300412

반응식

HRID 2300412 반응식
[F:1][C:2]([F:8])([F:7])[CH:3]=[CH:4][CH2:5][OH:6].[CH2:9]=[C:10]1[O:14][C:12](=[O:13])[CH2:11]1>O1CCCC1.C(OCC)C.C([O-])(=O)C.[Na+]>[C:12]([O:6][CH2:5]/[CH:4]=[CH:3]/[C:2]([F:8])([F:7])[F:1])(=[O:13])[CH2:11][C:10]([CH3:9])=[O:14]

참가 물질

6

실험 절차

To a refluxing solution of 4,4,4-trifluoro-2-buten-1-ol (10 g, 79 mmol) and sodium acetate (0.51 g, 6.2 mmol) in anhydrous tetrahydrofuran (27 mL) under nitrogen, a solution of diketene (6.7 mL, 43.1 mmol) in anhydrous tetrahydrofuran (14 mL) was added dropwise over a period of 1 hour. The reaction mixture was heated at reflux for an additional 30 min upon completion of the addition. Then, the reaction mixture mixture was cooled to room temperature and diluted with diethyl ether (100 mL). The resulting solution was washed with a saturated aqueous sodium chloride solution (2×20 mL) and the organic layer was dried over sodium sulfate, filtered and the solvent removed under reduced pressure. The brown residue was purified by column chromatography using a mixture 4:1 of hexane and ethyl acetate as eluent to afford 14.0 g (84% yield) of trans-4,4,4-trifluoro-2-buten-1-yl acetoacetate as a colorless liquid.

후처리

  1. temperatureThe reaction mixture was heated
  2. temperatureat reflux for an additional 30 min upon completion of the addition
  3. washThe resulting solution was washed with a saturated aqueous sodium chloride solution (2×20 mL)
  4. dry with materialthe organic layer was dried over sodium sulfate
  5. filtrationfiltered
  6. customthe solvent removed under reduced pressure
  7. customThe brown residue was purified by column chromatography

출처 및 근거

ORD 기록
ord-67b8eca8eae940b397db843fffd70999
출처 데이터셋
uspto-grants-2002_12
특허 번호
US06498180B1

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