Sodium Hydroxide → N-(carboxymethyl)-N-[3-(decyloxy)benzoyl]glycine
Reaction equation
[OH-].[Na+].C[O:4][C:5](=[O:32])[CH2:6][N:7]([CH2:27][C:28]([O:30]C)=[O:29])[C:8](=[O:26])[C:9]1[CH:14]=[CH:13][CH:12]=[C:11]([O:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH3:25])[CH:10]=1>>[C:5]([CH2:6][N:7]([C:8](=[O:26])[C:9]1[CH:14]=[CH:13][CH:12]=[C:11]([O:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH3:25])[CH:10]=1)[CH2:27][C:28]([OH:30])=[O:29])([OH:32])=[O:4]Participants
3
Procedure
Sodium hydroxide hydrolysis of N-(2-methoxy-2-oxoethyl)-N-[3-(decyloxy)benzoyl]glycine methyl ester as in Example 4 gave N-(carboxymethyl)-N-[3-(decyloxy)benzoyl]glycine, mp 87°-90°.
Sources & evidence
- ORD record
- ord-16d61e05e5044b45b375b12f217c81f8
- Source dataset
- uspto-grants-1994_03
- Patent number