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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1084861Generated: November 2, 2026

Hydrochloric Acid → Ethyl 3-methyl-4-methoxy-7-benzoylbenzofuran-2-carboxylate

https://huagongshe.com/reaction/1084861

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantBenzoyl chlorideHCID 7412—
ReactantAluminum(III) ChlorideHCID 6451240—
ReactantEthyl 4-methoxy-3-methyl-2-benzofurancarboxylateHCID 9497663—
Solvent1,2-DichloroethaneHCID 11—
ProductEthyl 3-methyl-4-methoxy-7-benzoylbenzofuran-2-carboxylateHCID 15124007—

Reaction Steps

To a solution of ethyl 3-methyl-4-methoxybenzofuran-2-carboxylate (1.00 g, 4.27 mmol) and benzoyl chloride (1.80 g, 12.81 mmol) in 1,2-dichloroethane (12 mL) was added aluminum chloride (1.71 g, 12.81 mmol) in portions. The mixture was heated to reflux for 1.5 hours then allowed to cool and poured into 2N HCl (50 mL). The resulting mixture was extracted with methylene chloride (3×30 mL) and the combined extracts washed with saturated NaHCO3 (3×25 mL), dried (Na2SO4), and concentrated. The crude product was purified by preparative HPLC, using 25% ethyl acetate in hexane as eluant, to afford ethyl 3-methyl-4-methoxy-7-benzoylbenzofuran-2-carboxylate mp. 137°-139° C.; 1H NMR d 1.27 (2H, t, J=6 Hz), 2.67 (3H, s), 3.95 (3H, s), 4.28 (2H, q, J=6 Hz), 6.66 (1H, d, J=8 Hz), 7.44 (3H, m), 7.72 (3H, m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05006549
Source datasetuspto-grants-1991_04
ORD IDord-4f739b9da9064a2c999752a0d28c0d85
Source noteuspto-grants-1991_04