반응 #2320114

ord-362a673cbda6434b830ef4a2e818229d

반응 방정식

FC(F)(F)c1cc(C2=CCN(Cc3ccccc3)CC2)ccc1Cl
1-Benzyl-4-(4-chloro-3-trifluoromethyl-phenyl)-1,2,3,6-tetrahydro-pyridine
Cl
hydrochloric acid
FC(F)(F)c1cc(C2CCN(Cc3ccccc3)CC2)ccc1Cl
title compound
수율 82.3%
FC(F)(F)c1cc(C2CCN(Cc3ccccc3)CC2)ccc1Cl
1-Benzyl-4-(4-chloro-3-trifluoromethyl-phenyl)-piperidine
수율 82.3%

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타for 1 h
  2. 2
    여과filtered through a pad of celite
  3. 3
    기타The solvent was evaporated in vacuum
  4. 4
    기타the residue was purified by flash chromatography (SiO2, CH2Cl2:MeOH, 9:1 (v/v))

실험 절차

1-Benzyl-4-(4-chloro-3-trifluoromethyl-phenyl)-1,2,3,6-tetrahydro-pyridine (1.45 g) was dissolved in methanol (40 ml). Concentrated hydrochloric acid (0.2 ml) and 50 mg Pd/C, were added. The resulting mixture was hydrogenated under a hydrogen gas pressure (40 psi) for 1 h and then filtered through a pad of celite. The solvent was evaporated in vacuum and the residue was purified by flash chromatography (SiO2, CH2Cl2:MeOH, 9:1 (v/v)) to give the pure title compound (1.2 g). MS m/z (relative intensity, 70 eV) 353 (M+, 16), 262 (20), 91 (bp), 65 (18), 56 (14).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: USRE041315E1uspto-grants-2010_05