反応式
O.NN.[CH3:4][N:5]1[CH:9]=[CH:8][CH:7]=[C:6]1[CH2:10][C:11]([O:13]C)=[O:12]>C(O)C>[CH3:4][N:5]1[CH:9]=[CH:8][CH:7]=[C:6]1[CH2:10][C:11]([OH:13])=[O:12]参加物
4
実験手順
Hydrazine monohydrate (65 ml) was added dropwise to a solution of methyl 1-methyl-1H-pyrrole-2-acetate (0.326 mol) in ethanol (300 ml) and the mixture was refluxed for 4 hours. The mixture was evaporated till dryness. The residue was taken up in dichloromethane and an aqueous potassium carbonate solution (10%) and extracted with dichloromethane. The organic layer was dried (MgSO4) and evaporated. The residue (48.8 g) was taken up in 1,1'-oxybisethane and the precipitate was filtered off, yielding 45.3 g (90%) of 1-methyl-1H-pyrrole-2-acetic acid, hydrazine (interm. 7).
後処理
- temperaturethe mixture was refluxed for 4 hours
- customThe mixture was evaporated till dryness
- extractionan aqueous potassium carbonate solution (10%) and extracted with dichloromethane
- dry with materialThe organic layer was dried (MgSO4)
- customevaporated
- filtrationthe precipitate was filtered off
出典と根拠
- ORDレコード
- ord-1606391d53524f5db959d205bbe2579e
- 出典データセット
- uspto-grants-1997_01
- 特許番号
- US05595988
関連ノート
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