反応式
[OH:1][C:2]([C:5]1[CH:14]=[CH:13][C:8]([C:9]([O:11][CH3:12])=[O:10])=[CH:7][CH:6]=1)([CH3:4])[CH3:3].[C:15]1(C)C=CC(S(O)(=O)=O)=CC=1>CO>[CH3:15][O:1][C:2]([C:5]1[CH:14]=[CH:13][C:8]([C:9]([O:11][CH3:12])=[O:10])=[CH:7][CH:6]=1)([CH3:3])[CH3:4]参加物
4
実験手順
To a solution of methyl 4-(1-hydroxy-1-methylethyl)benzoate (340 mg, 1.75 mmol) in methanol (20 mL) was added p-toluenesulfonic acid (70 mg, 0.37 mmol). The mixture was refluxed for 48 h, concentrated in vacuo, and the residue chromatographed (silica gel, 10% ethyl acetate/90% hexanes to 30% ethyl acetate/70% hexanes) to give 118 mg (32%) of the title compound.
後処理
- temperatureThe mixture was refluxed for 48 h
- concentrationconcentrated in vacuo
- customthe residue chromatographed (silica gel, 10% ethyl acetate/90% hexanes to 30% ethyl acetate/70% hexanes)
出典と根拠
- ORDレコード
- ord-67685d60245a469fa18ca99d6e3ab644
- 出典データセット
- uspto-grants-2001_11
- 特許番号
- US06313122B1
関連ノート
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