1-Benzyl-3-acetamidopyrrolidine → 3-Acetamidopyrrolidine
反応式
[C:1]([NH:4][CH:5]1[CH2:9][CH2:8][N:7](CC2C=CC=CC=2)[CH2:6]1)(=[O:3])[CH3:2]>C(O)C.O.[C].[Pd]>[C:1]([NH:4][CH:5]1[CH2:9][CH2:8][NH:7][CH2:6]1)(=[O:3])[CH3:2]参加物
5
実験手順
To a solution of the above 3-acetylamino-1-benzylpyrrolidine (4.0 g) in ethanol (30 ml) was added 10% palladium-carbon (0.8 g) in water (1 ml). The mixture was shaken at room temperature for 22 hours under hydrogen pressure of 55 p.s.i. using Parr hydrogenator. The catalyst was filtered off and the solvent was distilled off under reduced pressure. The residue was dissolved in chloroform and dried over anhydrous magnesium sulfate, followed by distilling off the solvent to give 3-acetylaminopyrrolidine (2.3 g) as oil.
後処理
- filtrationThe catalyst was filtered off
- distillationthe solvent was distilled off under reduced pressure
- dissolutionThe residue was dissolved in chloroform
- dry with materialdried over anhydrous magnesium sulfate
- distillationby distilling off the solvent
出典と根拠
- ORDレコード
- ord-004e964c05094558bb944e448effad59
- 出典データセット
- uspto-grants-1989_08
- 特許番号
- US04853469
反応ノート
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