4-Methylbenzaldehyde → p-Tolyl(2-(trifluoromethyl)phenyl)methanol
Reaction equation
[F:1][C:2]([F:12])([F:11])[C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][C:4]=1[Mg]Br.[C:13]1([CH3:21])[CH:18]=[CH:17][C:16]([CH:19]=[O:20])=[CH:15][CH:14]=1.FC(F)(F)C1C=C(Cl)C=CC=1C(O)C1C=CC=CC=1>>[F:1][C:2]([F:12])([F:11])[C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][C:4]=1[CH:19]([OH:20])[C:16]1[CH:17]=[CH:18][C:13]([CH3:21])=[CH:14][CH:15]=1Participants
4
Procedure
This material was prepared from 2-(trifluoromethyl)phenylmagnesium bromide (16 mmol) and p-tolualdehyde (1.82 mL, 15 mmol) using the procedure described for compound (96) (4.28 g, 100%).
Sources & evidence
- ORD record
- ord-d05f8651193c4d94b238cc07cd1ed39b
- Source dataset
- uspto-grants-2009_03
- Patent number
- US07504522B2
Reaction notes
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