Reacción #324617

ord-7d867147ffd541b38140cb598cd36b86

Ecuación de reacción

Cc1cc(O)cc(C)c1Br
4-bromo-3,5-dimethylphenol
O=C([O-])[O-].[K+].[K+]
K2CO3
CC1(CBr)COC1
3-(bromomethyl)-3-methyloxetane
Cc1cc(OCC2(C)COC2)cc(C)c1Br
title compound
Cc1cc(OCC2(C)COC2)cc(C)c1Br
3-((4-Bromo-3,5-dimethylphenoxy)methyl)-3-methyloxetane

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Otropartitioned between saturated aqueous NaHCO3 solution and ethyl acetate
  2. 2
    ExtracciónThe aqueous phase is extracted with ethyl acetate
  3. 3
    Secadothe combined organic phases are dried (MgSO4)
  4. 4
    OtroThe solvent is evaporated
  5. 5
    Otrothe residue is chromatographed on silica gel (cyclohexane/ethyl acetate 100:0→70:30)

Procedimiento

To a solution of 4-bromo-3,5-dimethylphenol (3.0 g) and K2CO3 (5.5 g) in N,N-dimethylformamide (10 mL) is added 3-(bromomethyl)-3-methyloxetane (2.95 g). The mixture is stirred for 12 hours at room temperature and then partitioned between saturated aqueous NaHCO3 solution and ethyl acetate. The aqueous phase is extracted with ethyl acetate and the combined organic phases are dried (MgSO4). The solvent is evaporated and the residue is chromatographed on silica gel (cyclohexane/ethyl acetate 100:0→70:30) to give the title compound. Yield: 3.5 g; LC (method 4): tR=1.81 min; Mass spectrum (ESI+): m/z=285 [M+H]+.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08642585B2uspto-grants-2014_02