Reacción #43938

ord-d925f96ad2644afc88152e75846ea9ee

Ecuación de reacción

Cc1cc(O)cc(C)c1Br
4-bromo-3,5-dimethylphenol
CSCCCO
3-(methylthio)-1-propanol
CCCCP(CCCC)CCCC
tributylphosphine
O=C(N=NC(=O)N1CCCCC1)N1CCCCC1
1,1′-(azodicarbonyl)dipiperidine
CSCCCOc1cc(C)c(Br)c(C)c1
title compound
Rendimiento 87.0%
CSCCCOc1cc(C)c(Br)c(C)c1
2-bromo-1,3-dimethyl-5-[3-(methylthio)propoxy]benzene
Rendimiento 87.0%

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Filtraciónthe insoluble substance was filtered off
  2. 2
    Concentraciónthe filtrate was concentrated under reduced pressure
  3. 3
    OtroThe residue was purified by silica gel column chromatography (ethyl acetate:hexane=0:100-25:75)

Procedimiento

To a solution of 4-bromo-3,5-dimethylphenol (4.02 g, 20.0 mmol), 3-(methylthio)-1-propanol (2.12 g, 20.0 mmol) and tributylphosphine (7.97 mL, 32.0 mmol) in toluene (320 mL) was added 1,1′-(azodicarbonyl)dipiperidine (8.07 g, 32.0 mmol), and the mixture was stirred at room temperature for 18 hr under nitrogen atmosphere. Hexane (160 mL) was added to the reaction mixture, the insoluble substance was filtered off, and the filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate:hexane=0:100-25:75) to give the title compound (5.03 g, yield 87%) as a pale-yellow oil.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07732626B2uspto-grants-2010_06