Sodium Hydroxide → HCID 58822579, compound
Reaction equation
C([O:3][C:4](=[O:39])[C@@H:5]([O:37][CH3:38])[CH2:6][C:7]1[CH:12]=[CH:11][C:10]([O:13][CH2:14][CH2:15][CH2:16][O:17][C:18]2[CH:23]=[CH:22][C:21]([C:24]3[C:29]4[S:30][C:31]5[CH:36]=[CH:35][CH:34]=[CH:33][C:32]=5[C:28]=4[CH:27]=[CH:26][CH:25]=3)=[CH:20][CH:19]=2)=[CH:9][CH:8]=1)C.[OH-].[Na+]>>[CH:27]1[C:28]2[C:32]3[CH:33]=[CH:34][CH:35]=[CH:36][C:31]=3[S:30][C:29]=2[C:24]([C:21]2[CH:20]=[CH:19][C:18]([O:17][CH2:16][CH2:15][CH2:14][O:13][C:10]3[CH:9]=[CH:8][C:7]([CH2:6][C@H:5]([O:37][CH3:38])[C:4]([OH:39])=[O:3])=[CH:12][CH:11]=3)=[CH:23][CH:22]=2)=[CH:25][CH:26]=1Participants
3
Procedure
The title compound was prepared from (2S)-3-{4-[3-(4-Dibenzothiophen-4-yl-phenoxy)-propoxy]-phenyl}-2-methoxy-propionic acid ethyl ester (Step A) by Standard Hydrolysis procedure C (NaOH). MS (ES) for C31H28O5S [M+NH4]+: 530.
Sources & evidence
- ORD record
- ord-787bca0414f1461db975bb0fbe8e9428
- Source dataset
- uspto-grants-2007_03
- Patent number
- US07192982B2
Reaction notes
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