反応式
[CH3:1][C:2]1[C:6]2[CH:7]=[CH:8][CH:9]=[CH:10][C:5]=2[O:4][C:3]=1[C:11]([OH:13])=[O:12].[C:14](Cl)(=O)C(Cl)=O.CO>CN(C=O)C.C1COCC1>[CH3:1][C:2]1[C:6]2[CH:7]=[CH:8][CH:9]=[CH:10][C:5]=2[O:4][C:3]=1[C:11]([O:13][CH3:14])=[O:12]参加物
6
実験手順
To a solution of 3-methyl-benzofuran-2-carboxylic acid (0.98 g, 5.6 mmol) and catalytic amount of DMF (5 drops) in THF (25 ml) was added oxalyl chloride (0.53 ml, 6.1 mmol). After stirring the solution for 1 h at room temperature, methanol (20 ml) and TEA (7.0 ml) were added. The reaction mixture was stirred overnight at room temperature, then concentrated and dissolved in ethyl acetate (100 ml) and washed with aqueous sodium bicarbonate solution (100 ml). The organic layer was dried over sodium sulfate and concentrated to provide crude methyl 3-methylbenzofuran-2-carboxylate (1.0 g, 5.3 mmol) as a tan solid, which was used without further purification.
後処理
- stirringThe reaction mixture was stirred overnight at room temperature
- concentrationconcentrated
- dissolutiondissolved in ethyl acetate (100 ml)
- washwashed with aqueous sodium bicarbonate solution (100 ml)
- dry with materialThe organic layer was dried over sodium sulfate
- concentrationconcentrated
出典と根拠
- ORDレコード
- ord-c6b527b2c1074afab8ad5326b4ecda9b
- 出典データセット
- uspto-grants-2008_05
- 特許番号
- US07368572B2
関連ノート
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