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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 12854생성일: 2026년 10월 26일

Ethyl formate → Ethyl 2-formyl-3-oxopropanoate

https://huagongshe.com/reaction/12854

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl formateHCID 8025—
반응물Ethyl 3,3-diethoxypropionateHCID 66389—
반응물HCID 178418922HCID 178418922—
용매TetrahydrofuranHCID 8028—
생성물Ethyl 2-formyl-3-oxopropanoateHCID 11029955100.1%

반응 조건

온도0 °C

반응 단계

Ethyl 3,3-diethoxypropionate (100 g, 525.7 mmol) was dissolved in THF (360 ml) at room temp. Ethyl formate (175.1 ml, 2.1 mol) was added at room temp. The solution was cooled in an ice-bath to 0° C. and tBuOK (1M solution in THF, 1,156 ml, 1.156 mol) was added via an addition funnel slowly over 30 min, maintaining internal temperature below 5° C. The color changed instantly from colorless to dark orange. The reaction mixture was allowed to warm up to room temp. and stirred for 2 h. The reaction was allowed to stir at room temp. for 18 h. The reaction mixture was concentrated in vacuo and 1 L of solvent was removed. The remaining brownish solution with white solid in it was cooled in an ice-bath and hydrochloric acid (6N, 200 ml) was added to adjust pH=3, maintaining internal temperature below 20° C. The resulting bright yellow suspension was then warmed up to room temp. and stirred for 1 h. Additional 700 ml solvent was removed in vacuo at room temp. Water (400 ml) was added to dissolve all the white solid and ethyl acetate (500 ml) was added and the mixture transferred to a separatory funnel. The aqueous was extracted once with ethyl acetate (200 ml). The combined organic extracts was washed once with brine (100 ml). After drying over MgSO4 and concentrating in vacuo, 2-formyl-3-oxo-propionic acid ethyl ester (75.85 g) was obtained as yellow oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07728029B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-f162d2aee57f4371ba5eb6e5a8135f3d
출처 메모uspto-grants-2010_06