反应 #1810824

ord-58cd6dd3f0924ee499d3256960bc9e9e

反应方程式

CC(C)(C)OC(=O)N1CC=C(c2ccc(C(F)(F)F)cc2)CC1
4-(4-trifluoromethyl-phenyl)-3,6-dihydro-2H-pyridine-1-carboxylic acid tert-butyl ester
O=C(O)C(F)(F)F
trifluoroacetic acid
FC(F)(F)c1ccc(C2=CCNCC2)cc1
title compound
FC(F)(F)c1ccc(C2=CCNCC2)cc1
4-(4-Trifluoromethyl-phenyl)-1,2,3,6-tetrahydro-pyridine

反应条件

温度
40°CELSIUS
详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    浓缩then concentrated
  2. 2
    workup.ADDITIONtreated with water/NaOH
  3. 3
    萃取extracted with dichloromethane
  4. 4
    洗涤The combined organic phases were washed with saturated NaCl
  5. 5
    干燥dried with MgSO4
  6. 6
    其他evaporated

实验过程

A mixture of 0.52 mmol 4-(4-trifluoromethyl-phenyl)-3,6-dihydro-2H-pyridine-1-carboxylic acid tert-butyl ester in 2 ml dichloromethane was treated with 0.2 ml trifluoroacetic acid. The mixture was stirred at 40° C. for 3 hrs then concentrated and treated with water/NaOH and extracted with dichloromethane. The combined organic phases were washed with saturated NaCl, dried with MgSO4 and evaporated to yield the title compound. MS (m/e): 228.3 (MH+, 100%)

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07485637B2uspto-grants-2009_02