Water → (2-(Cyclohexyl(methoxy)methyl)-5-(trifluoromethyl)phenyl)methanol

HRID 2075055

反応式

HRID 2075055 の反応式
[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

5

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

  1. extractionthe mixture was extracted with ethyl acetate
  2. washCombined organic layers were washed with brine
  3. dry with materialdried over sodium sulfate
  4. concentrationconcentrated in vacuo
  5. 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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