Sodium Hydroxide → HCID 58822781, compound
Reaction equation
C([O:8][C:9](=[O:36])[C:10]1[CH:15]=[CH:14][C:13]([O:16][CH2:17][CH2:18][CH2:19][O:20][C:21]2[CH:26]=[CH:25][C:24]([CH2:27][C@@H:28]([C:31]([O:33]CC)=[O:32])[O:29][CH3:30])=[CH:23][CH:22]=2)=[CH:12][CH:11]=1)C1C=CC=CC=1.[OH-].[Na+]>>[C:31]([C@@H:28]([O:29][CH3:30])[CH2:27][C:24]1[CH:23]=[CH:22][C:21]([O:20][CH2:19][CH2:18][CH2:17][O:16][C:13]2[CH:14]=[CH:15][C:10]([C:9]([OH:36])=[O:8])=[CH:11][CH:12]=2)=[CH:26][CH:25]=1)([OH:33])=[O:32]Participants
3
Procedure
The title compound was prepared from (2S)-4-{3-[4-(2-Ethoxycarbonyl-2-methoxy-ethyl)-phenoxy]-propoxy}-benzoic acid benzyl ester (Step A) by Standard Hydrolysis procedure C (NaOH). MS (ES) for C20H22O7 [M+Na]+: 397.
Sources & evidence
- ORD record
- ord-424f5e4e0d1f46b7bafa5e85053fda8a
- Source dataset
- uspto-grants-2007_03
- Patent number
- US07192982B2
Reaction notes
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