1-(Bromomethyl)-2-(trifluoromethyl)benzene → Toluene
Reaction equation
Br[CH2:2][C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][C:4]=1[C:9]([F:12])([F:11])[F:10].[N:13]1([C:19]2[N:20]=[N:21][CH:22]=[CH:23][N:24]=2)[CH2:18][CH2:17][NH:16][CH2:15][CH2:14]1>>[F:10][C:9]([F:12])([F:11])[C:4]1[CH:5]=[CH:6][CH:7]=[CH:8][C:3]=1[CH2:2][N:16]1[CH2:15][CH2:14][N:13]([C:19]2[N:20]=[N:21][CH:22]=[CH:23][N:24]=2)[CH2:18][CH2:17]1.[C:3]1([CH3:2])[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1Participants
4
Procedure
Compound 5 is prepared from 1-bromomethyl-2-trifluoromethyl-benzene and intermediate 5a according to synthesis method 2 in refluxing toluene (33% yield).
Workup
- customaccording to synthesis method 2
Sources & evidence
- ORD record
- ord-4b0b56fce1b14a60b311f2a446477f7a
- Source dataset
- uspto-grants-2015_02
- Patent number
- US08962837B2
Reaction notes
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