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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1738682Generated: October 30, 2026

Hydrochloric Acid → 5-Cyano-2-[2-(4-methoxyphenyl)ethyl]-3-benzofurancarboxylic acid

https://huagongshe.com/reaction/1738682

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
ReactantBromineHCID 24408—
Reactant3-Acetyl-2-[2-(4-methoxyphenyl)ethyl]-5-benzofurancarbonitrileHCID 21844431—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
Product5-Cyano-2-[2-(4-methoxyphenyl)ethyl]-3-benzofurancarboxylic acidHCID 2184439434.6%

Reaction Steps

5.2 g of sodium hydroxide was dissolved in 30 ml of water, and the solution was cooled to a temperature of 0° C. or below. With stirring, to this were added dropwise 2.7 ml of bromine and then 40 ml of a dioxane solution containing 4.14 g of 3-acetyl-2-[2-(4-methoxyphenyl)ethyl]-5-benzofurancarbonitrile obtained in the above step d). The resulting mixture was stirred at 0° C. for 45 minutes with ice cooling for 1 hour. The resulting reaction solution was mixed with water, adjusted to pH 2 with concentrated hydrochloric acid, and then extracted with chloroform. The resulting organic layer was washed with water and dried to distill off the solvent. Thereafter, the resulting residue was purified by subjecting it to silica gel column chromatography using chloroform as an eluant, thereby obtaining 1.44 g of 5-cyano-2-[2-(4-methoxyphenyl)ethyl]-3-benzofurancarboxylic acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05962695
Source datasetuspto-grants-1999_10
ORD IDord-f8e1688da9cd4f8c85f1f4adb2837598
Source noteuspto-grants-1999_10