Reaction equation
[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]Participants
3
Procedure
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.
Workup
- temperaturewas heated
- temperatureat reflux for 2 hours
- concentrationwas concentrated in vacuo
- distillationwas distilled (0.8 mm Hg, 68° C.)
Sources & evidence
- ORD record
- ord-8d502b49ae6b464793197a75442691c1
- Source dataset
- uspto-grants-2011_09
- Patent number
- US08012969B2
Linked notes
Loading…