反応式
C([N:8]1[CH2:12][CH2:11][CH:10]([N:13]2[C:17](=[O:18])[C:16]3=[CH:19][CH:20]=[CH:21][CH:22]=[C:15]3[C:14]2=[O:23])[CH2:9]1)C1C=CC=CC=1.[ClH:24]>C(O)C.[C].[Pd]>[ClH:24].[NH:8]1[CH2:12][CH2:11][CH:10]([N:13]2[C:17](=[O:18])[C:16]3=[CH:19][CH:20]=[CH:21][CH:22]=[C:15]3[C:14]2=[O:23])[CH2:9]1参加物
5
実験手順
12.70 g of N-(1-benzylpyrrolidin-3-yl)phthalimide was dissolved in 100 ml of ethanol and then subjected to hydrogenating decomposition with addition of 1.0 g of 10% palladium-carbon and 5.2 ml of concentrated hydrochloric acid at 60° C. under 1 atm. After 12 hours, the catalyst was filtered out and the solvent was distilled off to obtain 11.03 g of N-(3-pyrrolidyl)phthalimide hydrochloride.
後処理
- filtrationthe catalyst was filtered out
- distillationthe solvent was distilled off
出典と根拠
- ORDレコード
- ord-e5136a72017c48b5930c678cec053f52
- 出典データセット
- uspto-grants-1991_09
- 特許番号
- US05047417
関連ノート
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