Acetic Anhydride → 3-Acetyl-5-(3,4-dimethoxyphenyl)-2-oxazolidinone
反応式
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH:11]2[O:15][C:14](=[O:16])[NH:13][CH2:12]2)[CH:6]=[CH:7][C:8]=1[O:9][CH3:10].[C:17](OC(=O)C)(=[O:19])[CH3:18]>N1C=CC=CC=1>[C:17]([N:13]1[CH2:12][CH:11]([C:5]2[CH:6]=[CH:7][C:8]([O:9][CH3:10])=[C:3]([O:2][CH3:1])[CH:4]=2)[O:15][C:14]1=[O:16])(=[O:19])[CH3:18]参加物
4
実験手順
8.9 mmol of 5-(3,4-dimethoxyphenyl)-2-oxazolidinone is combined with 10 ml. of acetic anhydride and 5 ml. of pyridine and heated for 5 hours to 100°. After concentrating the reaction mixture, it is recrystallized from ethyl acetate, thus obtaining 3-acetyl-5-(3,4-dimethoxyphenyl)-2-oxazolidinone in a 73% yield, m.p. 175°-182°.
後処理
- concentrationAfter concentrating the reaction mixture, it
- customis recrystallized from ethyl acetate, thus obtaining 3-acetyl-5-(3,4-dimethoxyphenyl)-2-oxazolidinone in a 73% yield, m.p. 175°-182°
出典と根拠
- ORDレコード
- ord-97ea86f2edc5482ea8e366bc7dbf8b27
- 出典データセット
- uspto-grants-1980_01
- 特許番号
- US04186129
反応ノート
読み込み中…