Sodium Hydroxide → HCID 18951532, compound
Reaction equation
[OH-].[Na+].C[O:4][C:5](=[O:50])[C:6]1[CH:11]=[CH:10][C:9]([O:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH3:30])=[CH:8][C:7]=1[O:31][CH2:32][CH2:33][CH2:34][O:35][C:36]1[CH:41]=[CH:40][C:39]([O:42][CH2:43][C:44]2[CH:49]=[CH:48][CH:47]=[CH:46][CH:45]=2)=[CH:38][CH:37]=1>>[CH2:13]([O:12][C:9]1[CH:10]=[CH:11][C:6]([C:5]([OH:50])=[O:4])=[C:7]([O:31][CH2:32][CH2:33][CH2:34][O:35][C:36]2[CH:41]=[CH:40][C:39]([O:42][CH2:43][C:44]3[CH:45]=[CH:46][CH:47]=[CH:48][CH:49]=3)=[CH:38][CH:37]=2)[CH:8]=1)[CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH3:30]Participants
3
Procedure
Sodium hydroxide hydrolysis of 4-(octadecyloxy)-2-[3-[4-(phenylmethoxy)phenoxy]propoxy]benzoic acid methyl ester gave 4-(octadecyloxy)-2-[3-[4-(phenylmethoxy)phenoxy]propoxy]benzoic acid (88% yield, mp 102°-104°).
Sources & evidence
- ORD record
- ord-e21caed045b1487a9d1b9bd372c9ddef
- Source dataset
- uspto-grants-1994_12
- Patent number
- US05374772
Reaction notes
Loading…