Reacción #1986

ord-e94dfad47a4a48328c7cf02bef7e5975

Ecuación de reacción

OCC1(C(F)(F)F)CCN(Cc2ccccc2)C1
compound
OCC1(C(F)(F)F)CCN(Cc2ccccc2)C1
1-benzyl-3-trifluoromethylpyrrolidine-3-methanol
c1ccncc1
pyridine
Cc1ccc(S(=O)(=O)Cl)cc1
p-toluenesulfonyl chloride
c1ccncc1
pyridine
Cc1ccccc1S(=O)(=O)OCC1(C(F)(F)F)CCN(Cc2ccccc2)C1
title compound
Cc1ccccc1S(=O)(=O)OCC1(C(F)(F)F)CCN(Cc2ccccc2)C1
1-benzyl-3-trifluoromethyl-3-(toluenesulfonyloxymethyl)pyrrolidine

Condiciones de reacción

Temperatura
0°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Lavadowashed with water and brine
  2. 2
    Otrodried
  3. 3
    OtroRemoval of the solvent

Procedimiento

The compound from step 456b (1.61 g) was dissolved in dry pyridine, and the solution was cooled to 0° C. To this was added 1.458 g of p-toluenesulfonyl chloride in 4 mL of dry pyridine, and the reaction was stirred at 0.C for 4 days. The mixture was diluted with 300 mL of methylene chloride, then washed with water and brine and dried. Removal of the solvent gave 2.81 g of the title compound.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05726182uspto-grants-1998_03