Iodine → 4,4-Difluoro-2-iodocyclohex-2-en-1-one
反応式
[F:1][C:2]1([F:9])[CH2:7][CH2:6][C:5](=[O:8])[CH:4]=[CH:3]1.C(=O)([O-])[O-].[K+].[K+].[I:16]I>CN(C1C=CN=CC=1)C.C1COCC1.O>[F:1][C:2]1([F:9])[CH2:7][CH2:6][C:5](=[O:8])[C:4]([I:16])=[CH:3]1参加物
6
実験手順
To a solution of the 4,4-difluorocyclohex-2-en-1-one (1.0 g, 7.57 mmol) prepared in Example 88b in a THF-water mixed solvent (1:1; 20 mL), potassium carbonate (1.30 g, 9.41 mmol), iodine (2.9 g, 11.4 mmol) and DMAP (0.56 g, 4.58 mmol) were added, and the reaction solution was stirred at room temperature for 30 minutes. The reaction solution was subjected to extraction with ethyl acetate (20 mL). The thus obtained organic layer was washed with an aqueous sodium thiosulfate solution (20 mL) and dried over anhydrous sodium sulfate. After vacuum concentration, the residue was purified with silica gel chromatography (hexane/ethyl acetate=9:1) to yield the title compound (1.46 g, 75%) as a light brown oil.
後処理
- extractionThe reaction solution was subjected to extraction with ethyl acetate (20 mL)
- washThe thus obtained organic layer was washed with an aqueous sodium thiosulfate solution (20 mL)
- dry with materialdried over anhydrous sodium sulfate
- concentrationAfter vacuum concentration
- customthe residue was purified with silica gel chromatography (hexane/ethyl acetate=9:1)
出典と根拠
- ORDレコード
- ord-547c4213c6b74cfeacd14d029d8c36cc
- 出典データセット
- uspto-grants-2014_11
- 特許番号
- US08889741B2
反応ノート
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