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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 252804Generated: October 30, 2026

Ethyl bromoacetate → Ethyl 5-methyl-1-benzofuran-2-carboxylate

https://huagongshe.com/reaction/252804

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromoacetateHCID 7748—
ReactantPotassium CarbonateHCID 11430—
ReactantBenzaldehyde, 2-hydroxy-5-methyl-HCID 69184—
SolventDimethylformamideHCID 6228—
ProductEthyl 5-methyl-1-benzofuran-2-carboxylateHCID 1315701331%

Reaction Steps

To a stirred suspension of 2-hydroxy-5-methylbenzaldehyde (5 g, 36.7 mmol) and K2CO3 (12.7 g, 91.8 mmol) in DMF (30 mL), ethyl bromoacetate (4.07 ml, 36.7 mmol) was added drop-wise. This mixture was allowed to stir for two hours under nitrogen at room temperature, and was then heated to 80° C. and stirred overnight. The reaction was quenched with H2O to form a precipitate which was collected by filtration and purified by flash chromatography (eluent 5% EtOAc in hexane) to give the title compound 25 (2.30 g, 31%). 1H-NMR (CDCl3) δ: 1.45 (t, J=7.0 Hz, 3H); 2.47 (s, 3H); 4.45 (q, J=7.0 Hz, 2H); 7.26 (m, 1H); 7.46 (m, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07868205B2
Source datasetuspto-grants-2011_01
ORD IDord-b930c7e699374458a498e877b4abae1a
Source noteuspto-grants-2011_01