Reaktion #595370

ord-41752e8eda6a478d996396309c9f08f6

Reaktionsgleichung

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

Reaktionsbedingungen

Temperatur
80°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeThe solvent was removed in vacuo
  2. 2
    workup.ADDITIONthe residue was diluted with EtOAc
  3. 3
    Waschenwashed with H2O, brine
  4. 4
    Trocknendried over anhydrous Na2SO4
  5. 5
    Einengenconcentrated
  6. 6
    WaschenThe resulting crude solid was washed with PE

Vorschrift

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).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US09095583B2uspto-grants-2015_08