Réaction #2320113

ord-19a7d5580ccf4fa4ac655dccca1ef96f

Équation de réaction

OC1(c2ccc(Cl)c(C(F)(F)F)c2)CCN(Cc2ccccc2)CC1
1-Benzyl-4-(4-chloro-3-trifluoromethyl-phenyl)-piperidine-4-ol
O=C(O)C(F)(F)F
trifluoroacetic acid
FC(F)(F)c1cc(C2=CCN(Cc3ccccc3)CC2)ccc1Cl
1-Benzyl-4-(4-chloro-3-trifluoromethyl-phenyl)-1,2,3,6-tetrahydro-pyridine

Solvants

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Températurerefluxed for 24 hours
  2. 2
    AutreThe phases were separated
  3. 3
    Lavagethe organic phase was washed with two portions of 10%-Na2CO3
  4. 4
    Séchagedried (MgSO4)
  5. 5
    Filtrationfiltered
  6. 6
    Autreevaporated to dryness

Mode opératoire

1-Benzyl-4-(4-chloro-3-trifluoromethyl-phenyl)-piperidine-4-ol (1.5 g) was dissolved trifluoroacetic acid (35 ml) and refluxed for 24 hours and then CH2Cl2 (200 ml) was added. The phases were separated and then the organic phase was washed with two portions of 10%-Na2CO3, dried (MgSO4), filtered and evaporated to dryness. Yield 1.5 g. MS m/z (relative intensity, 70 eV) 351 (M+, 27), 172 (9), 92 (11), 91 (bp), 65 (21).

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: USRE041315E1uspto-grants-2010_05