Lithium Hydroxide → HCID 21935858, compound
Reaction equation
C([O:3][C:4](=[O:40])[C:5]([CH3:39])([O:7][C:8]1[CH:13]=[CH:12][C:11]([O:14][CH2:15][C:16]2[C:17]([CH3:37])=[N:18][C:19]([C:26]3[CH:31]=[CH:30][C:29]([O:32][C:33]([F:36])([F:35])[F:34])=[CH:28][CH:27]=3)=[CH:20][C:21]=2[C:22]([F:25])([F:24])[F:23])=[CH:10][C:9]=1[CH3:38])[CH3:6])C.[Li+].[OH-]>>[CH3:39][C:5]([O:7][C:8]1[CH:13]=[CH:12][C:11]([O:14][CH2:15][C:16]2[C:17]([CH3:37])=[N:18][C:19]([C:26]3[CH:27]=[CH:28][C:29]([O:32][C:33]([F:36])([F:35])[F:34])=[CH:30][CH:31]=3)=[CH:20][C:21]=2[C:22]([F:23])([F:24])[F:25])=[CH:10][C:9]=1[CH3:38])([CH3:6])[C:4]([OH:40])=[O:3]Participants
3
Procedure
In analogy to the procedure described in example 26C], 2-methyl-2-{2-methyl-4-[2-methyl-6-(4-trifluoromethoxy-phenyl)-4-trifluoromethyl-pyridin-3-ylmethoxy]-phenoxy}-propionic acid ethyl ester was treated with LiOH to obtain the title compound as colorless solid.
Sources & evidence
- ORD record
- ord-824462946939426b916f48b3246d2e03
- Source dataset
- uspto-grants-2006_10
- Patent number
- US07115611B2
Reaction notes
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