Diketene → HCID 86758741、化合物

HRID 2300412

反応式

HRID 2300412 の反応式
[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]

参加物

6

実験手順

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.

後処理

  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

出典と根拠

ORDレコード
ord-67b8eca8eae940b397db843fffd70999
出典データセット
uspto-grants-2002_12
特許番号
US06498180B1

関連ノート

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