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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1173792Generated: October 25, 2026

Hydrochloric Acid → 3-(2,2,2-Trifluoroethoxymethyl)benzofuran-2-carboxylic acid

https://huagongshe.com/reaction/1173792

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant2,2,2-TrifluoroethanolHCID 6409—
ReactantSodium HydroxideHCID 14798—
ReactantSodium hydrideHCID 24758—
ReactantMethyl 3-(bromomethyl)-2-benzofurancarboxylateHCID 100838—
SolventDimethylformamideHCID 6228—
Product3-(2,2,2-Trifluoroethoxymethyl)benzofuran-2-carboxylic acidHCID 28943207—

Reaction Steps

Sodium hydride (15 mg, 0.56 mmol) was suspended in anhydrous DMF and stirred under N2(g). 2,2,2-Trifluoroethanol (270 μL, 3.7 mmol) was added and after stirring the reaction mixture for 15-20 min., 3-bromomethylbenzofuran-2-carboxylic acid methyl ester was added. After 8 h, 1N NaOH (aq.) was added and the reaction mixture was stirred for 10-15 min. The reaction mixture was acidified reaction to pH 3 with aqueous hydrochloric acid and the product was extracted with EtOAc. The organic layer was dried organic over Na2SO4 and concentrated in vacuo to give 3-(2,2,2-trifluoroethoxymethyl)benzofuran-2-carboxylic acid (38 mg) which was then used without purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07834054B2
Source datasetuspto-grants-2010_11
ORD IDord-fd11af11c1764737acd675a774dfac70
Source noteuspto-grants-2010_11