HCID 24780974, compound → HCID 24781284, compound
Reaction equation
[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]([CH3:10])([CH3:9])[C:6]([OH:8])=[O:7]>C(O)CCC.O>[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)[O:18][CH2:1][CH2:2][CH2:3][CH3:11])[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
Reactant 1
Product 1
Reagents, catalysts & solvents 1
Procedure
This compound was prepared following the general procedure E, using 2-[2,6-dimethyl-4-[3-[4-(methylthio)phenyl]-3-hydroxypropyl]phenoxy]-2-methylpropanoic acid in 50/50 butanol/water at 70° C. for 32 hours;
Workup
- customThis compound was prepared
- customat 70° C.
- customfor 32 hours
Sources & evidence
- ORD record
- ord-f5ba641e4a974cc8b9189881301f7d6e
- Source dataset
- uspto-grants-2012_09
- Patent number
- US08258182B2
Reaction notes
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