Reacción #5235

ord-4a3dc28a00854038bc8f00c5c9d2d330

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    workup.STIRRINGThe reaction mixture was stirred for 24 h
  2. 2
    Extracciónextracted with ethyl acetate three times
  3. 3
    SecadoThe combined organic layers were dried over magnesium sulfate
  4. 4
    Filtraciónfiltered
  5. 5
    OtroSolvent was removed in vacuo
  6. 6
    FiltraciónTrituration with ether-hexanes (1:9) and filtration

Procedimiento

1-(Cyclopropylmethyl)-4-(2'-(4"-fluorophenyl)-2'-oxoethyl)piperidine (Example 429, 1.0 g, 3.6 mmol) was mixed with dry tetrahydrofuran (10 mL). A solution of phenyl magnesium bromide in ether (3.0M, 3 mL, 9 mmol) was added with stirring. The reaction mixture was stirred for 24 h; poured onto a saturated NH4Cl solution and extracted with ethyl acetate three times. The combined organic layers were dried over magnesium sulfate and filtered. Solvent was removed in vacuo. Trituration with ether-hexanes (1:9) and filtration afforded the title compound, a solid, which was dried in vacuo (0.9 g) mp 115°-116° C.; Anal.: Calcd for C23H28FNO: C, 77.36, H, 7.90, N, 3.92, F, 5.32; Found: C, 77.47, 77.41, H, 8.00, 7.92, N, 3.42, 3.52, F, 5.09.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05243048uspto-grants-1993_09