反応式
[N+:1]([C:4]1[CH:5]=[C:6]([CH:9]=[CH:10][CH:11]=1)[CH:7]=O)([O-:3])=[O:2].[CH3:12][O:13][C:14](=[O:22])[CH2:15]P(OC)(OC)=O.C[O-].[Na+].Cl>CN(C=O)C>[N+:1]([C:4]1[CH:5]=[C:6](/[CH:7]=[CH:15]/[C:14]([O:13][CH3:12])=[O:22])[CH:9]=[CH:10][CH:11]=1)([O-:3])=[O:2]参加物
6
実験手順
To a solution of 3-nitro-benzaldehyde (15 g, 0.1 mol), (dimethoxy-phosphoryl)-acetic acid methyl ester (27 g, 0.148 mol) in DMF (100 ml) was added NaOMe (10.7 g 0.198 mol). The reaction was monitored by TLC. After reaction was completed, the reaction mixture was adjusted to pH=1 with aqueous HCl solution and evaporated. The resulting solid was washed with water to afford (E)-methyl 3-(3-nitrophenyl)acrylate as a yellow solid (20.14 g, 98%).
後処理
- customAfter reaction
- customevaporated
- washThe resulting solid was washed with water
出典と根拠
- ORDレコード
- ord-21764d9679824589a2b348fab79c75d6
- 出典データセット
- uspto-grants-2014_12
- 特許番号
- US08906909B2
関連ノート
読み込み中…