Trifluoroacetic acid → 2-(2-Bromo-4-(3-oxo-3-(5-(4-(trifluoromethyl)phenyl)thien-2-yl)propyl)-phenoxy)butanoic acid

HRID 416083Notes

Reaction equation

HRID 416083 reaction equation
[Br:1][C:2]1[CH:18]=[C:17]([CH2:19][CH2:20][C:21](=[O:37])[C:22]2[S:23][C:24]([C:27]3[CH:32]=[CH:31][C:30]([C:33]([F:36])([F:35])[F:34])=[CH:29][CH:28]=3)=[CH:25][CH:26]=2)[CH:16]=[CH:15][C:3]=1[O:4][CH:5]([CH2:13][CH3:14])[C:6]([O:8]C(C)(C)C)=[O:7].FC(F)(F)C(O)=O>>[Br:1][C:2]1[CH:18]=[C:17]([CH2:19][CH2:20][C:21](=[O:37])[C:22]2[S:23][C:24]([C:27]3[CH:28]=[CH:29][C:30]([C:33]([F:36])([F:35])[F:34])=[CH:31][CH:32]=3)=[CH:25][CH:26]=2)[CH:16]=[CH:15][C:3]=1[O:4][CH:5]([CH2:13][CH3:14])[C:6]([OH:8])=[O:7]

Participants

3

Procedure

2-(2-Bromo-4-(3-oxo-3-(5-(4-(trifluoromethyl)phenyl)thien-2-yl)propyl)-phenoxy)butanoic acid is prepared from tert-butyl 2-(2-bromo-4-(3-oxo-3-(5-(4-(trifluoromethyl)phenyl)thien-2-yl)propyl)phenoxy)butanoate according to general procedure E using 17 equivalents of trifluoroacetic acid.

Sources & evidence

ORD record
ord-803f858f69e642799b3b61736131a1b7
Source dataset
uspto-grants-2012_01
Patent number
US08088819B2

Reaction notes

Loading…