反応式
[CH:1]1([CH:7]([O:27][CH3:28])[C:8]2[CH:22]=[CH:21][C:20]([C:23]([F:26])([F:25])[F:24])=[CH:19][C:9]=2[CH2:10][O:11][Si](C(C)(C)C)(C)C)[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.CCCC[N+](CCCC)(CCCC)CCCC.[F-].O>C1COCC1>[CH:1]1([CH:7]([O:27][CH3:28])[C:8]2[CH:22]=[CH:21][C:20]([C:23]([F:26])([F:25])[F:24])=[CH:19][C:9]=2[CH2:10][OH:11])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6]1参加物
実験手順
To a solution of (2-(cyclohexyl(methoxy)methyl)-5-(trifluoromethyl)benzyloxy)(tert-butyl)dimethylsilane (1.13 g, 2.4 mmol) in THF (5 mL) at room temperature was added TBAF in THF (1.0 M, 4.8 mL, 4.8 mmol). The mixture was stirred at room temperature overnight. Water was added and the mixture was extracted with ethyl acetate. Combined organic layers were washed with brine, dried over sodium sulfate and concentrated in vacuo. The residue was purified by chromatography over 25+M Biotage silica column (eluted with 0-30% ethyl acetate in heptane) to afford the title compound (633.9 mg, 88%). 1H NMR (400 MHz, CDCl3) δ ppm 0.91-1.27 (m, 6H) 1.63-1.70 (m, 3H) 1.72-1.81 (m, 1H) 2.07 (d, J=12.86 Hz, 1H) 2.33-2.42 (m, 1H) 3.18 (s, 3H) 4.10 (d, J=7.88 Hz, 1H) 4.78 (dd, J=5.81, 3.32 Hz, 2H) 7.43 (d, J=7.88 Hz, 1H) 7.55 (d, J=8.30 Hz, 1H) 7.69 (s, 1H).
後処理
- extractionthe mixture was extracted with ethyl acetate
- washCombined organic layers were washed with brine
- dry with materialdried over sodium sulfate
- concentrationconcentrated in vacuo
- customThe residue was purified by chromatography over 25+M Biotage silica column (eluted with 0-30% ethyl acetate in heptane)
出典と根拠
- ORDレコード
- ord-5fafb6bc74174aba9782d556b7a48049
- 出典データセット
- uspto-grants-2011_04
- 特許番号
- US07919506B2
関連ノート
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