Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1058574Generated: October 26, 2026

Hydrochloric Acid → Ethyl 5-hydroxybenzofuran-2-carboxylate

https://huagongshe.com/reaction/1058574

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthanethiolHCID 6343—
Reactant2-Benzofurancarboxylic acid, 5-methoxy-, ethyl esterHCID 521283—
ReactantAluminum(III) ChlorideHCID 6451240—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductEthyl 5-hydroxybenzofuran-2-carboxylateHCID 2222863277%

Reaction Steps

To a mixture of aluminum chloride (6.3 g, 47.7 mmol) and ethanethiol (4.5 g, 72.9 mmol) in dichloromethane (81 mL) at 0° C. was added ethyl 5-methoxybenzofuran-2-carboxylate (3.0 g, 13.6 mmol). After stirring for 16 h at room temperature, the mixture was poured into water, acidified with 3N HCl and extracted with dichloromethane (2x). The organic layers were combined, washed with brine, collected, dried (MgSO4), filtered and concentrated. The residue was purified by column chromatography (silica gel, ethyl acetate/hexane) to yield the title compound as a white solid (2.16 g, 77%). 1H NMR (400 MHz, CDCl3) δ 7.45 (m, 2H), 7.08 (m, 1H), 7.02 (m, 1H), 5.35 (s b, 1H), 4.44 (q, 2H), 1.42 (t, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06518267B1
Source datasetuspto-grants-2003_02
ORD IDord-5292b85848ff4c28acefb19b4c2edb28
Source noteuspto-grants-2003_02