Ammonia → 5-(2-Hydroxyethyl)pyrrolidin-2-one
反応式
C(O[CH:5]1[CH2:12][CH2:11][O:10][C:8](=[O:9])[CH2:7][CH2:6]1)(=O)C.[NH3:13]>>[OH:10][CH2:11][CH2:12][CH:5]1[NH:13][C:8](=[O:9])[CH2:7][CH2:6]1参加物
3
実験手順
22.4 g of 4-acetoxycaprolactone were stirred for 1 hour at 330° C. in an autoclave together with 100 g of 25% strength aqueous ammonia. After cooling and depressurizing the autoclave, the reaction product was concentrated on a rotary evaporator (40° C./30 mbar) and purified by short path distillation. In this case, 10.1 g of 5-hydroxyethylpyrrolidone were obtained (61%, based on the 4-acetoxycaprolactone employed) and identified by NMR spectroscopy.
後処理
- temperatureAfter cooling
- concentrationthe reaction product was concentrated on a rotary evaporator (40° C./30 mbar)
- distillationpurified by short path distillation
出典と根拠
- ORDレコード
- ord-681a67c854174aa6978cc40b7d9e9217
- 出典データセット
- uspto-grants-1994_02
- 特許番号
- US05286875
反応ノート
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