Ethanol → N-chloroacetamidomethyl acrylamide N-acrylamidomethyl-2-oxopyrrolidine
Reaction equation
[Cl:1][CH2:2][C:3]([NH:5][CH2:6][NH:7][C:8](=[O:11])[CH:9]=[CH2:10])=[O:4].[C:12]([NH:16][CH2:17][N:18]1[CH2:22][CH2:21][CH2:20][C:19]1=[O:23])(=[O:15])[CH:13]=[CH2:14].C(O)C.N(C(C)(C)C#N)=NC(C)(C)C#N>O>[Cl:1][CH2:2][C:3]([NH:5][CH2:6][NH:7][C:8](=[O:11])[CH:9]=[CH2:10])=[O:4].[C:12]([NH:16][CH2:17][N:18]1[CH2:22][CH2:21][CH2:20][C:19]1=[O:23])(=[O:15])[CH:13]=[CH2:14]Participants
6
Procedure
18 g of N-chloroacetamidomethyl acrylamide, 18 g of acrylamidomethyl 2-oxopyrrolidine, 144 g of ethanol, 144 g of water and 1.8 g of azobis-iso-butyronitrile are placed in a reactor. The mixture is heated under a nitrogen blanket for 2 hours with constant stirring.
Workup
- temperatureThe mixture is heated under a nitrogen blanket for 2 hours with constant stirring
Sources & evidence
- ORD record
- ord-999f4e73c23942a3b612e5f1918bb1d4
- Source dataset
- uspto-grants-1989_08
- Patent number
- US04859460
Reaction notes
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