Reacción #312582

ord-f5a86ba414ad4793a8b3bf01c1c1e5cc

Ecuación de reacción

CC(=O)c1ccc(F)cc1F
2,4-difluoroacetophenone
COC(OC)OC
trimethyl ortho-formate
O=C([O-])O.[Na+]
sodium hydrogen carbonate
COC(C)(OC)c1ccc(F)cc1F
1-(1,1-dimethoxyethyl)-2,4-difluorobenzene

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    workup.ADDITIONwas added
  2. 2
    Otroreacted at 40° C. to 45° C. for 2 hours
  3. 3
    Extracciónwas then extracted with ethyl acetate
  4. 4
    LavadoAn extract was washed with water
  5. 5
    Otrodried on Na2SO4
  6. 6
    ConcentraciónThen, ethyl acetate was concentrated

Procedimiento

In a solution composed of 15.7 g of 2,4-difluoroacetophenone, 35 g of trimethyl ortho-formate and 15 g of methanol, 0.96g of p-toluenesulfonic acid was added, and reacted at 40° C. to 45° C. for 2 hours. This was added to an aqueous solution of 5% by mass sodium hydrogen carbonate, which was then extracted with ethyl acetate. An extract was washed with water, and dried on Na2SO4. Then, ethyl acetate was concentrated to yield 18.2 g of 1-(1,1-dimethoxyethyl)-2,4-difluorobenzene. It was confirmed that the 1-(1,1-dimethoxyethyl)-2,4-difluorobenzene had NMR data of (CDCl3, δppm) 1.62 (s, 3H), 3.9 (s, 6H), 6.74-6.9 (m, 2H), 7.56-7.7 (m, 1H) by NMR (supplied from Varian Technologies Japan Limited).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07556911B2uspto-grants-2009_07