反応式
[CH:1]1([OH:7])[CH2:6][CH2:5][CH2:4][CH:3]=[CH:2]1.N1C=CC=CC=1.[C:14](OC(=O)C)(=[O:16])[CH3:15]>>[C:14]([O:7][CH:1]1[CH2:6][CH2:5][CH2:4][CH:3]=[CH:2]1)(=[O:16])[CH3:15]参加物
4
反応条件
- 温度
- 0 °C
実験手順
To a solution of 2-cyclohexen-1-ol (16) (45.5 mmol, 5.02 mL) in pyridine (0.27 mol, 22 mL) at 0° C., acetic anhydride was added dropwise and the reaction mixture was stirred at 0° C. for ½ h. The ice bath was removed, and the mixture was stirred at room temperature overnight. The mixture was diluted with EtOAc, washed with HCl (1 N), saturated NaHCO3, brine, and concentrated in vacuo to give 6 g (94%) of the crude product 17 which was used in the next step without further purification. TLC with 20% EtOAc/Hexane, stained with 5% H2SO4/EtOH, Rf for (16): 0.4, Rf for (17): 0.8.
後処理
- customThe ice bath was removed
- stirringthe mixture was stirred at room temperature overnight
- additionThe mixture was diluted with EtOAc
- washwashed with HCl (1 N), saturated NaHCO3, brine
- concentrationconcentrated in vacuo
出典と根拠
- ORDレコード
- ord-9b69b1c899954ecc88c475798102edee
- 出典データセット
- uspto-grants-2014_11
- 特許番号
- US08889719B2
関連ノート
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