Reaktion #2320113

ord-19a7d5580ccf4fa4ac655dccca1ef96f

Reaktionsgleichung

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

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturrefluxed for 24 hours
  2. 2
    SonstigeThe phases were separated
  3. 3
    Waschenthe organic phase was washed with two portions of 10%-Na2CO3
  4. 4
    Trocknendried (MgSO4)
  5. 5
    Filtrationfiltered
  6. 6
    Sonstigeevaporated to dryness

Vorschrift

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).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: USRE041315E1uspto-grants-2010_05