Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1643728Generated: November 1, 2026

Potassium Carbonate → Ethyl 4-hydroxy-2-methylbenzofuran-6-carboxylate

https://huagongshe.com/reaction/1643728

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant6-Benzofurancarboxylic acid, 4-(acetyloxy)-2-methyl-, ethyl esterHCID 59560094—
SolventEthanolHCID 702—
SolventDichloromethaneHCID 6344—
ProductEthyl 4-hydroxy-2-methylbenzofuran-6-carboxylateHCID 1151406595%

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture of ethyl 4-(acetyloxy)-2-methyl-1-benzofuran-6-carboxylate in absolute ethanol (500 mL) and potassium carbonate (18 g, 0.13 mol) was stirred for 3 h at 60° C. The mixture was diluted with 500 mL of dichloromethane and the suspension was filtered. The precipitate was washed with 200 mL of dichloromethane. The combined solutions was washed with 200 mL of a 10% aqueous solution of citric acid and evaporated in vacuum to dryness. The crude product introduced into a silica gel column and eluted with hexane/ethyl acetate mixture (2:1) to give 20 g (91 mmol, 95%) of desired compound as a yellow solid. 1HNMR (DMSO d-6): 1.30 (t, 3H), 2.45 (s, 3H), 4.30 (qt, 2H), 6.65 (s, 1H), 7.28 (2, 1H) 7.53 (s, 1H), 10.25 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08119624B2
Source datasetuspto-grants-2012_02
ORD IDord-22bcc067fda64e6383ea8ca7df648d48
Source noteuspto-grants-2012_02