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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1909867생성일: 2026년 10월 26일

Citric Acid → 4-(4-chlorobenzyl)-4H-furo[3,2-b]pyrrole-5-carboxylic acid

https://huagongshe.com/reaction/1909867

반응식

참여 물질

역할이름HCID투입량
반응물Citric AcidHCID 311—
반응물Sodium hydrideHCID 24758—
반응물1-(Bromomethyl)-4-chlorobenzeneHCID 69329—
반응물methyl 4H-furo[3,2-b]pyrrole-5-carboxylateHCID 5082263—
용매DimethylformamideHCID 6228—
생성물4-(4-chlorobenzyl)-4H-furo[3,2-b]pyrrole-5-carboxylic acidHCID 3973379841.9%

반응 단계

To a mixture of sodium hydride (0.29 g, 55% dispersion in paraffin liquid) and DMF (10 mL) was added methyl 4H-furo[3,2-b]pyrrole-5-carboxylate (0.5 g) under ice-cooling, followed by stirring for 10 minutes and further 1-(bromomethyl)-4-chlorobenzene (0.81 g) was added thereto, followed by stirring at room temperature for 4 hours. To the reaction mixture was added a 10% aqueous citric acid solution (10 mL), followed by extraction with ethyl acetate. The organic layer was dried over anhydrous sodium sulfate and then concentrated under reduced pressure, and the residue was purified by silica gel column chromatography (hexane/ethyl acetate: 5/1-3/1) to obtain 4-(4-chlorobenzyl)-4H-furo[3,2-b]pyrrole-5-carboxylic acid (0.35 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08598355B2
출처 데이터셋uspto-grants-2013_12
ORD IDord-147052373a9a4f6f922197eb55206b96
출처 메모uspto-grants-2013_12