Sodium borohydride → HCID 24780974, compound
Reaction equation
[CH3:1][C:2]1[CH:14]=[C:13]([CH2:15][CH2:16][C:17]([C:19]2[CH:24]=[CH:23][C:22]([S:25][CH3:26])=[CH:21][CH:20]=2)=[O:18])[CH:12]=[C:11]([CH3:27])[C:3]=1[O:4][C:5]([CH3:10])([CH3:9])[C:6]([OH:8])=[O:7].[BH4-].[Na+]>>[CH3:1][C:2]1[CH:14]=[C:13]([CH2:15][CH2:16][CH:17]([C:19]2[CH:24]=[CH:23][C:22]([S:25][CH3:26])=[CH:21][CH:20]=2)[OH:18])[CH:12]=[C:11]([CH3:27])[C:3]=1[O:4][C:5]([CH3:9])([CH3:10])[C:6]([OH:8])=[O:7]Participants
3
Procedure
This compound was prepared following the general procedure D, using 2-[2,6-dimethyl-4-[3-[4-(methylthio)phenyl]-3-oxo-propyl]phenoxy]-2-methylpropanoic acid, and 3 equivalent amounts of sodium borohydride;
Workup
- customThis compound was prepared
Sources & evidence
- ORD record
- ord-9e9bbc5fa7014e1692e8a85e5e54429a
- Source dataset
- uspto-grants-2012_09
- Patent number
- US08258182B2
Reaction notes
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