Reacción #2358573

ord-fee12b97c0ea40b6aee4c63721f06aee

Ecuación de reacción

BrC(c1ccccc1)c1ccccc1
Diphenylmethyl bromide
C1COCCN1
morpholine
CCN(CC)CC
triethylamine
c1ccc(C(c2ccccc2)N2CCOCC2)cc1
title compound
Rendimiento 14.0%
c1ccc(C(c2ccccc2)N2CCOCC2)cc1
4-Benzhydrylmorpholine
Rendimiento 14.0%

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Concentraciónthe reaction mixture was concentrated in vacuo
  2. 2
    Otrothe resulting crude mixture was purified by column chromatography (10% ethyl acetate/hexanes)

Procedimiento

Diphenylmethyl bromide (211 mg, 0.877 mmol) was added to a solution of morpholine (23.9 μL, 0.274 mmol), triethylamine (130 μL, 0.932 mmol) and chloroform (1.4 mL) and was allowed to stir at room temperature. After 48 hr, the reaction mixture was concentrated in vacuo and the resulting crude mixture was purified by column chromatography (10% ethyl acetate/hexanes) to provide the title compound in 14% yield.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US09120744B2uspto-grants-2015_09