反応式
[F:1][C:2]1[CH:10]=[C:9]([I:11])[CH:8]=[CH:7][C:3]=1[C:4]([OH:6])=[O:5].[CH3:12][Si:13]([CH3:18])([CH3:17])[CH2:14][CH2:15]O>ClCCl.CN(C)C1C=CN=CC=1>[F:1][C:2]1[CH:10]=[C:9]([I:11])[CH:8]=[CH:7][C:3]=1[C:4]([O:6][CH2:15][CH2:14][Si:13]([CH3:18])([CH3:17])[CH3:12])=[O:5]参加物
実験手順
To a solution of 115.5 mg (0.4 mmol) of 2-fluoro-4-iodobenzoic acid (Compound B) in 10 mL of dichloromethane (under a blanket of argon) was added 91.5 mg (0.5 mmol) of 1-(3-dimethylaminopropyl-3-ethyl carbodiimide hydrochloride) and 53 mg (0.4 mmol) of 4-dimethylaminopyridine. To this reaction mixture was added 0.16 ml (132 mg, 1.1 mmol) of 2-trimethylsilylethanol and the resultant mixture was allowed to stir at ambient temperature for 23 hours. The reaction mixture was extracted between ethyl ether and water and the layers were separated. The aqueous phase was washed with ethyl ether (2×50 mL) and the organic phases were combined. The combined organic phase was washed with brine, dried over MgSO4, filtered and concentrated in vacuo to a clear, colorless oil. Purification by flash chromatography (silica, 3% ethyl acetate in hexane) gave the title compound as a clear, colorless oil.
後処理
- extractionThe reaction mixture was extracted between ethyl ether and water
- customthe layers were separated
- washThe aqueous phase was washed with ethyl ether (2×50 mL)
- washThe combined organic phase was washed with brine
- dry with materialdried over MgSO4
- filtrationfiltered
- concentrationconcentrated in vacuo to a clear, colorless oil
- customPurification by flash chromatography (silica, 3% ethyl acetate in hexane)
出典と根拠
- ORDレコード
- ord-0c4e45554f2a47ea83143b4db26ef270
- 出典データセット
- uspto-grants-2003_12
- 特許番号
- US06660755B2
関連ノート
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