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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1291004Generated: October 31, 2026

Dimethyl Sulfate → HCID 10847938, compound

https://huagongshe.com/reaction/1291004

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfateHCID 6497—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 54714549HCID 54714549—
SolventAcetoneHCID 180—
ProductHCID 10847938HCID 1084793891%

Reaction Steps

Ethyl 5-cyano-3-hydroxy-2-benzofurancarboxylate (200 mg, 0.866 mmol), dimethyl sulfate (131 mg, 1.04 mmol) and potassium carbonate (132 mg, 0.953 mmol) were added to acetone (140 ml), and the mixture was refluxed under heating for 1.5 hours. Low boiling matters were distilled away from the reaction mixture under reduced pressure and water (200 ml) was added to the residue, which was followed by extraction with ethyl acetate. The extract was washed with water and saturated brine, and dried over anhydrous magnesium sulfate. After filtration, low boiling matters were distilled away from the filtrate under reduced pressure to give 193 mg of ethyl 5-cyano-3-methoxy-2-benzofurancarboxylate (91%). The obtained compound (170 mg, 0.694 mmol) was dissolved in methanol (5 ml) and potassium hydroxide (160 mg, 2.86 mmol) was added, which was followed by refluxing under heating for 45 minutes. Low boiling matters were distilled away from the reaction mixture under reduced pressure and 1N hydrochloric acid was added to the residue to adjust the pH to 2-3. The resulting precipitate was collected by filtration to give 123 mg of 5-cyano-3-methoxy-2-benzofurancarboxylic acid as a colorless solid (82%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05753670
Source datasetuspto-grants-1998_05
ORD IDord-1503bb99b7aa49c787fcb706ecd038ef
Source noteuspto-grants-1998_05