Hydrochloric Acid → 4-(3-(Trifluoromethyl)Phenyl)Piperidine
Reaction equation
C([N:8]1[CH2:13][CH:12]=[C:11]([C:14]2[CH:19]=[CH:18][CH:17]=[C:16]([C:20]([F:23])([F:22])[F:21])[CH:15]=2)[CH2:10][CH2:9]1)C1C=CC=CC=1.Cl>>[F:23][C:20]([F:21])([F:22])[C:16]1[CH:15]=[C:14]([CH:11]2[CH2:10][CH2:9][NH:8][CH2:13][CH2:12]2)[CH:19]=[CH:18][CH:17]=1Participants
3
Procedure
Beginning with 1-Benzyl-4-(3-trifluoromethyl-phenyl)-1,2,3,6-tetrahydro-pyridine (1.44 g), 1 g of the title compound as HCl salt was recovered by the procedure described in preparation 9. m.p. 202° C. (HCl); MS m/z (rel. intensity, 70 eV) 229 (M+, 44), 228 (33), 83 (12), 57 (54), 56 (bp).
Sources & evidence
- ORD record
- ord-f0268d600b224104b953b50c4b923c8c
- Source dataset
- uspto-grants-2016_08
- Patent number
- USRE046117E1
Reaction notes
Loading…