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HRID 713736생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/713736

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물2,2,2-TrifluoroethanolHCID 6409—
반응물Sodium HydroxideHCID 14798—
반응물Sodium hydrideHCID 24758—
반응물Methyl 3-(bromomethyl)-2-benzofurancarboxylateHCID 100838—
용매DimethylformamideHCID 6228—
생성물3-(2,2,2-Trifluoroethoxymethyl)benzofuran-2-carboxylic acidHCID 28943207—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09186347B1
출처 데이터셋uspto-grants-2015_11
ORD IDord-0b81eb893faa4199a158c8e195a94d9e
출처 메모uspto-grants-2015_11