Acetic Anhydride → 2-Acetoxy-3-methoxybenzaldehyde
反応式
[O:1]=[CH:2][C:3]1[CH:11]=[CH:10][CH:9]=[C:6]([O:7][CH3:8])[C:4]=1[OH:5].CN(C1C=CC=CN=1)C.[C:21](OC(=O)C)(=[O:23])[CH3:22]>Cl>[C:21]([O:5][C:4]1[C:6]([O:7][CH3:8])=[CH:9][CH:10]=[CH:11][C:3]=1[CH:2]=[O:1])(=[O:23])[CH3:22]参加物
5
実験手順
To a solution of o-vanillin (10.1 g) and a catalytic quantity (0.8 g) of dimethylaminopyridine in N-diisopropylethyl amine (23 mL) at 0° C. was added acetic anhydride (8 mL). The solution was stirred overnight, poured into 2N hydrochloric acid (100 mL), extracted with dichloromethane and the solvent removed in vacuo to afford a yellow solid. Recrystallization from ethanol yielded yellow crystals (10.9 g, 85%): m.p. 75.4-76.2° C., lit17 m.p. 76° C.; EIMS m/z 194 (M+), 152, 106, 43.
後処理
- extractionextracted with dichloromethane
- customthe solvent removed in vacuo
- customto afford a yellow solid
- customRecrystallization from ethanol yielded yellow crystals (10.9 g, 85%)
出典と根拠
- ORDレコード
- ord-6b9024bc3b2949aa9c629344e94e9e1a
- 出典データセット
- uspto-grants-2004_08
- 特許番号
- US06777578B2
反応ノート
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