反応式
[NH:1]1[CH2:5][CH2:4][CH2:3][C:2]1=[O:6].[C:7](OC(=O)C)(=[O:9])[CH3:8]>>[C:7]([N:1]1[CH2:5][CH2:4][CH2:3][C:2]1=[O:6])(=[O:9])[CH3:8]参加物
3
実験手順
A mixture of 112 g of 2-pyrrolidinone (9) and 249 mL of acetic anhydride was heated at reflux for 2 hours. The resultant mixture was allowed to cool to room temperature, was concentrated in vacuo, and was distilled (0.8 mm Hg, 68° C.) to provide 160 g of N-acetyl-2-pyrrolidinone (4) in 96% yield.
後処理
- temperaturewas heated
- temperatureat reflux for 2 hours
- concentrationwas concentrated in vacuo
- distillationwas distilled (0.8 mm Hg, 68° C.)
出典と根拠
- ORDレコード
- ord-8d502b49ae6b464793197a75442691c1
- 出典データセット
- uspto-grants-2011_09
- 特許番号
- US08012969B2
関連ノート
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