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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 332616생성일: 2026년 10월 25일

Hydrochloric Acid → 5-Hydroxymethyl-3-furancarboxylic acid ethyl ester

https://huagongshe.com/reaction/332616

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물WaterHCID 962—
반응물TriethylamineHCID 8471—
반응물Ethyl chloroformateHCID 10928—
반응물Sodium borohydrideHCID 4311764—
반응물4-Ethoxycarbonylfuran-2-carboxylic acidHCID 53429231—
용매TetrahydrofuranHCID 8028—
생성물5-Hydroxymethyl-3-furancarboxylic acid ethyl esterHCID 5947873679%

반응 단계

4-Ethoxycarbonylfuran-2-carboxylic acid (0.47 g, 2.53 mmol) was dissolved in tetrahydrofuran (10 mL), triethylamine (0.53 mL, 3.80 mmol) and ethyl chloroformate (0.29 mL, 3.04 mmol) were added at 0° C., and the mixture was stirred at room temperature for 1 hour. The reaction mixture was filtered through celite, water (0.23 mL, 12.7 mmol) and sodium borohydride (0.19 g, 5.06 mmol) were added to the filtrate, and the mixture was stirred overnight. 1N Hydrochloric acid was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine, dried over anhydrous sodium sulfate and concentrated under reduced pressure. The obtained residue was purified by silica gel column chromatography (hexane/ethyl acetate=50/50) to give the title compound (0.34 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08877805B2
출처 데이터셋uspto-grants-2014_11
ORD IDord-65eda0e008bb4d8eb24d5cbd8b19000b
출처 메모uspto-grants-2014_11