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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1916645Generated: October 29, 2026

Ethyl bromoacetate → Ethyl (5-bromobenzofuran)-2-carboxylate

https://huagongshe.com/reaction/1916645

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromoacetateHCID 7748—
ReactantSodium CarbonateHCID 10340—
Reactant5-BromosalicylaldehydeHCID 72863—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductEthyl (5-bromobenzofuran)-2-carboxylateHCID 735184—

Reaction Conditions

Temperature80 °C

Reaction Steps

13.8 g (100 mmol) Na2CO3 are added to a solution of 4.02 g (20.0 mmol) 5-bromo-salicylaldehyde and 2.26 mL (20.0 mmol, 98%) ethyl bromoacetate in 50 mL DMF. The reaction mixture is heated to 80° C. and stirred for 2 h at this temperature. It is diluted with 200 mL water, the aqueous phase is extracted three times with 100 mL tert-butylmethylether and the combined organic extracts are washed twice with 50 mL water. The organic phase is dried over MgSO4, filtered through activated charcoal and the solvent is eliminated i.vac.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08618132B2
Source datasetuspto-grants-2013_12
ORD IDord-af8a151465c641a1965b75762ae374e0
Source noteuspto-grants-2013_12