Sodium Hydroxide → 9-[3-(4-Chlorophenyl)-2-oxo-4-phenyl-4-imidazolin-1-yl] pelargonic acid
Reaction equation
C[O:2][C:3](=[O:31])[CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][N:12]1[CH:16]=[C:15]([C:17]2[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=2)[N:14]([C:23]2[CH:28]=[CH:27][C:26]([Cl:29])=[CH:25][CH:24]=2)[C:13]1=[O:30].[OH-].[Na+]>CO>[Cl:29][C:26]1[CH:27]=[CH:28][C:23]([N:14]2[C:15]([C:17]3[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=3)=[CH:16][N:12]([CH2:11][CH2:10][CH2:9][CH2:8][CH2:7][CH2:6][CH2:5][CH2:4][C:3]([OH:31])=[O:2])[C:13]2=[O:30])=[CH:24][CH:25]=1Participants
4
Procedure
The product is produced as described in example 18 from 4.4 g of 9-[3-(4-chlorophenyl)-2-oxo-4-phenyl-4-imidazolin-1-yl] pelargonic acid methyl ester and 0.4 g of NaOH in 20 cc. of methanol. Further purification by chromatography on silicic acid gel using chloroform as eluant.
Workup
- customThe product is produced
- customFurther purification by chromatography on silicic acid gel
Sources & evidence
- ORD record
- ord-b34f8abfafb845369a006d1eefc8445b
- Source dataset
- uspto-grants-1982_09
- Patent number
- US04349684
Reaction notes
Loading…