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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 430784Generated: October 26, 2026

Dimethylformamide → Ethyl 7-methoxy-1-benzofuran-2-carboxylate

https://huagongshe.com/reaction/430784

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantEthyl chloroacetateHCID 7751—
Reactanto-VanillinHCID 8991—
ReactantPotassium CarbonateHCID 11430—
SolventWaterHCID 962—
ProductEthyl 7-methoxy-1-benzofuran-2-carboxylateHCID 52128448%

Reaction Conditions

Temperature120 °C

Reaction Steps

To N,N-dimethylformamide (300 ml), o-vanillin (25.2 g), ethyl chloroacetate (23.5 ml) and potassium carbonate (45 mg) were added and the resulting mixture was stirred at 120° C. for 14 hours. The reaction mixture was filtered to remove insoluble inorganic salts, and 1N hydrochloric acid (50 ml) was added to the mixture to stop the reaction. Distilled water (250 ml) was added and the resulting mixture was extracted 4 times with totally 150 ml of ethyl acetate containing 15% of n-hexane. The organic layers were washed with distilled water (100 ml) and with saturated brine (100 ml), and dried over anhydrous sodium sulfate. The sodium sulfate was removed by filtration and the solvent was concentrated to dryness under reduced pressure. The residue was purified by column chromatography (solvent: n-hexane/ethyl acetate=10/1 to 5/1) using silica gel to obtain the desired compound (17.4 g, yield: 48%) in the form of colorless needle-shaped crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06323235B1
Source datasetuspto-grants-2001_11
ORD IDord-e4b60001689a4e48aa41680344af977e
Source noteuspto-grants-2001_11