1-(4-(Trifluoromethyl)phenyl)ethan-1-one → 3-(4-Phenylthiophen-2-yl)-1-(4-(trifluoromethyl)phenyl)prop-2-en-1-one
Reaction equation
[C:1]1([C:7]2[CH:8]=[C:9]([CH:12]=O)[S:10][CH:11]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[F:14][C:15]([F:26])([F:25])[C:16]1[CH:21]=[CH:20][C:19]([C:22](=[O:24])[CH3:23])=[CH:18][CH:17]=1>>[C:1]1([C:7]2[CH:8]=[C:9]([CH:12]=[CH:23][C:22]([C:19]3[CH:20]=[CH:21][C:16]([C:15]([F:14])([F:25])[F:26])=[CH:17][CH:18]=3)=[O:24])[S:10][CH:11]=2)[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=1Participants
3
Procedure
By a procedure similar to that of example 1.59.1, starting from 4-phenylthiophene-2-carbaldehyde and p-(trifluoromethyl)acetophenone, 3-(4-phenylthiophen-2-yl)-1-(4-(trifluoromethyl)phenyl)prop-2-en-1-one was obtained as yellow solid.
Sources & evidence
- ORD record
- ord-a9d0e634f97b424d9a84369c56a7651f
- Source dataset
- uspto-grants-2014_12
- Patent number
- US08912186B2
Reaction notes
Loading…