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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1177324Generated: November 1, 2026

Ethanol → ethyl 4-hydroxy-1-benzothiophene-6-carboxylate

https://huagongshe.com/reaction/1177324

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 86624768HCID 86624768—
SolventDichloromethaneHCID 6344—
Productethyl 4-hydroxy-1-benzothiophene-6-carboxylateHCID 1137905537%

Reaction Conditions

Temperature60 °C

Reaction Steps

4-(Acetyloxy)-1-benzothiophene-6-carboxylate was dissolved in absolute ethanol (200 mL). Potassium carbonate (14 g, 0.1 mol) was added. The reaction mixture was stirred for 3 h at 60° C. and diluted with 200 mL of dichloromethane. The suspension was filtered. The precipitate was washed by 100 mL of dichloromethane. The combined solutions were washed by 200 mL of a 10% aqueous solution of citric acid and evaporated in vacuum to dryness. The obtained crude product was chromatographed on a layer of silica gel (150×100 mm) with hexane/ethyl acetate mixture, 2:1 as eluent to give 6.5 g (29 mmol, 37%) of ethyl 4-hydroxy-1-benzothiophene-6-carboxylate as a cream-colored solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07842713B2
Source datasetuspto-grants-2010_11
ORD IDord-54eeefd0629b4fbaa12c6dbcf7de28cc
Source noteuspto-grants-2010_11