Hydrochloric Acid → HCID 23324916, compound
Reaction equation
C[O:2][C:3](=[O:20])[CH2:4][CH2:5][CH:6]1[CH:10]([C:11]2[CH:16]=[CH:15][C:14]([Cl:17])=[C:13]([Cl:18])[CH:12]=2)[CH2:9][C:8](=[O:19])[NH:7]1.C[O:22][C:23](=[O:40])[CH2:24][CH:25]([C:32]1[CH:37]=[CH:36][C:35]([Cl:38])=[C:34]([Cl:39])[CH:33]=1)[CH:26]1[CH2:30][CH2:29][C:28](=[O:31])[NH:27]1.Cl>[OH-].[Na+]>[Cl:39][C:34]1[CH:33]=[C:32]([CH:25]([CH:26]2[CH2:30][CH2:29][C:28](=[O:31])[NH:27]2)[CH2:24][C:23]([OH:40])=[O:22])[CH:37]=[CH:36][C:35]=1[Cl:38].[Cl:18][C:13]1[CH:12]=[C:11]([CH:10]2[CH2:9][C:8](=[O:19])[NH:7][CH:6]2[CH2:5][CH2:4][C:3]([OH:20])=[O:2])[CH:16]=[CH:15][C:14]=1[Cl:17]Participants
6
Reactant 3
Product 2
Reagents, catalysts & solvents 1
Procedure
A solution of 34.1 g of 3-(3,4-dichlorophenyl)-5-oxo-2-pyrrolidinepropanoic acid methyl ester and β-(3,4-dichlorophenyl)-5-oxo-2-pyrrolidinepropanoic acid methyl ester in aqueous sodium hydroxide solution (1 N, 108 ml) is heated to 60° C. for four hours. Excess aqueous hydrochloric acid (1 N, 120 ml) is added and the solution is concentrated under reduced pressure to give β-(3,4-dichlorophenyl)-5-oxo-2-pyrrolidinepropanoic acid and 3-(3,4-dichlorophenyl)-5-oxo-2-pyrrolidinepropanoic acid.
Workup
- concentrationthe solution is concentrated under reduced pressure
Sources & evidence
- ORD record
- ord-67128ce32f2b40c995d5a38e3cde904f
- Source dataset
- uspto-grants-1986_04
- Patent number
- US04584313
Reaction notes
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