Reacción #595370

ord-41752e8eda6a478d996396309c9f08f6

Ecuación de reacción

Cc1cc(C(=O)O)c(F)cc1Br
4-bromo-2-fluoro-5-methylbenzoic acid
O=S(Cl)Cl
SOCl2
CO
CH3OH
COC(=O)c1cc(C)c(Br)cc1F
title compound
COC(=O)c1cc(C)c(Br)cc1F
methyl 4-bromo-2-fluoro-5-methylbenzoate

Condiciones de reacción

Temperatura
80°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    OtroThe solvent was removed in vacuo
  2. 2
    workup.ADDITIONthe residue was diluted with EtOAc
  3. 3
    Lavadowashed with H2O, brine
  4. 4
    Secadodried over anhydrous Na2SO4
  5. 5
    Concentraciónconcentrated
  6. 6
    LavadoThe resulting crude solid was washed with PE

Procedimiento

To a solution of 4-bromo-2-fluoro-5-methylbenzoic acid (i-2a) (1.87 g, 8 mmol) in CH3OH (50 mL) at 0° C. was added SOCl2 (6 mL, 80 mmol) dropwise. Then the mixture was heated to 80° C. for 2 h. The solvent was removed in vacuo and the residue was diluted with EtOAc and washed with H2O, brine, dried over anhydrous Na2SO4, and concentrated. The resulting crude solid was washed with PE to give the title compound as a yellow solid. 1H NMR (400 MHz, CDCl3) δ 7.80 (1H, d), 7.37 (1H, d), 3.92 (3H, s), 2.39 (3H, s).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US09095583B2uspto-grants-2015_08