1-(Chloromethyl)-2-(trifluoromethyl)benzene → HCID 70002050, compound
Reaction equation
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([C:11]2[C@H:20]3[C@H:15]([CH2:16][CH2:17][CH2:18][CH2:19]3)[C:14](=[O:21])[NH:13][N:12]=2)[CH:6]=[CH:7][C:8]=1[O:9][CH3:10].[F:22][C:23]([F:33])([F:32])[C:24]1[CH:31]=[CH:30][CH:29]=[CH:28][C:25]=1[CH2:26]Cl.C(N1N=C(C2C=CC(OC)=C(OC)C=2)[C@H]2[C@H](CCCC2)C1=O)C1C=CC=CC=1>>[CH3:1][O:2][C:3]1[CH:4]=[C:5]([C:11]2[C@H:20]3[C@H:15]([CH2:16][CH2:17][CH2:18][CH2:19]3)[C:14](=[O:21])[N:13]([CH2:26][C:25]3[CH:28]=[CH:29][CH:30]=[CH:31][C:24]=3[C:23]([F:22])([F:32])[F:33])[N:12]=2)[CH:6]=[CH:7][C:8]=1[O:9][CH3:10]Participants
4
Procedure
Prepared from compound 1 and 2-trifluoromethylbenzylchloride as described for compound 78. Purified by chromatography (dichloromethane). Crystallized from petroleum ether (60°-95° C.). M.p. 87°-88° C.
Workup
- customPurified by chromatography (dichloromethane)
- customCrystallized from petroleum ether (60°-95° C.)
Sources & evidence
- ORD record
- ord-47319389b9bb4153ada7aa34240a337f
- Source dataset
- uspto-grants-2000_08
- Patent number
- US06103718
Reaction notes
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