Reaktion #1827480

Reaktionsgleichung

6-bromo-2-hydroxybenzaldehyde

ethyl chloroacetate

potassium carbonate

→

4-bromo-2-ethoxycarbonylbenzofuran

Ausbeute 70.0%

Lösungsmittel

N,N-dimethylformamide

Reaktionsbedingungen

Aufarbeitung

1. 1
   FiltrationInsoluble materials were filtered off
2. 2
   Sonstigethe solvent was removed under reduced pressure
3. 3
   workup.ADDITIONEthyl acetate and water were added to the residue
4. 4
   SonstigeThe layers were separated
5. 5
   Waschenthe organic layer was washed with water and brine
6. 6
   Trocknendried over magnesium sulfate
7. 7
   Sonstigeevaporated in vacuo
8. 8
   SonstigeThe residue was purified by column chromatography on silica gel eluting with a mixture of hexane and toluene (1:1)

Vorschrift

A mixture of 6-bromo-2-hydroxybenzaldehyde (4.48 g), ethyl chloroacetate (3.55 g) and powdered potassium carbonate (6.16 g) in N,N-dimethylformamide (56 ml) was stirred at 120° C. for one hour. Insoluble materials were filtered off and the solvent was removed under reduced pressure. Ethyl acetate and water were added to the residue, and the mixture was acidified by hydrochloric acid solution. The layers were separated and the organic layer was washed with water and brine, dried over magnesium sulfate and evaporated in vacuo. The residue was purified by column chromatography on silica gel eluting with a mixture of hexane and toluene (1:1) to afford 4-bromo-2-ethoxycarbonylbenzofuran (4.20 g).

Quelle