Reaktion #9739

ord-2e4f1814c45a4d49ad767afa4112ca37

Reaktionsgleichung

O=S([O-])O.[Na+]
sodium hydrogen sulfite
[Na+].[O-][Br+2]([O-])[O-]
sodium bromate
COC(=O)c1cc(-c2ccc(C(F)(F)F)cc2)oc1C
methyl 2-methyl-5-[4-(trifluoromethyl)phenyl]-3-furoate
COC(=O)c1cc(-c2ccc(C(F)(F)F)cc2)oc1C
intermediate 23
COC(=O)c1cc(-c2ccc(C(F)(F)F)cc2)oc1C
methyl 2-methyl-5-[4-(trifluoromethyl)phenyl]-3-furoate
CCOCC
diethylether
COC(=O)c1cc(-c2ccc(C(F)(F)F)cc2)oc1CBr
title compound
COC(=O)c1cc(-c2ccc(C(F)(F)F)cc2)oc1CBr
methyl 2-(bromomethyl)-5-[4-(trifluoromethyl)phenyl]-3-furoate

Reaktionsbedingungen

Temperatur
10°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Waschenwashed with fresh water
  2. 2
    WaschenThe organic layer was washed with 10% sodium thiosulfite solution
  3. 3
    Trocknendried over magnesium sulfate
  4. 4
    SonstigeThe crude product isolated by evaporation
  5. 5
    Sonstigepurified by flash column chromatography

Vorschrift

A solution of sodium bromate (8.14 g) in water (27 ml) was treated with a suspension of methyl 2-methyl-5-[4-(trifluoromethyl)phenyl]-3-furoate (intermediate 23, 5.12 g) in cyclohexane (36 ml). The system was cooled to <10° C. in ice/water bath and treated with a solution of sodium hydrogen sulfite (9.4 g) in water (54 ml) in a drop-wise manner over 30 minutes. The reaction was allowed to warm up to 10° C. for 2 hours and then poured into diethylether (400 ml) and washed with fresh water. The organic layer was washed with 10% sodium thiosulfite solution and dried over magnesium sulfate. The crude product isolated by evaporation, was pre-adsorbed onto silica and purified by flash column chromatography using 39:1 cyclohexane:ethyl acetate as eluent to give the title compound as a white powder.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07091237B2uspto-grants-2006_08