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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1063809생성일: 2026년 10월 25일

Diethyl Oxalate → Ethyl 3-cyclopentyl-3-oxopropanoate

https://huagongshe.com/reaction/1063809

반응식

참여 물질

역할이름HCID투입량
반응물Diethyl OxalateHCID 7268—
반응물Cyclopentyl methyl ketoneHCID 22326—
반응물SodiumHCID 5360545—
용매EthanolHCID 702—
생성물Ethyl 3-cyclopentyl-3-oxopropanoateHCID 11159709—

반응 조건

온도60 °C

반응 단계

Sodium pellets (3.1 g, 135 mmol) were dissolved in ethanol (100 ml) under nitrogen at room temperature and a solution of diethyloxalate (18.4 ml, 135 mmol) and 1-cyclopentylethanone (16.7 g, 149 mmol) was added dropwise at room temperature over 30 minutes. The reaction was diluted with ethanol (100 ml), heated to 60° C. and stirred at this temperature for 2 hours. After cooling to room temperature the reaction was poured onto ice-cold 2N HCl (200 ml) and extracted with diethylether (300 ml) and ethyl acetate (300 ml). The combined organic extracts were dried over MgSO4, concentrated under reduced pressure and the residue was purified by flash column chromatography on silica gel eluting with pentane:ethyl acetate (6:1, by volume) to give 3-cyclopentyl-3-oxo-propionc acid ethyl ester (23.8 g) as an orange oil. 1H NMR (400 MHz, CDCl3): δ=14.38-14.65 (1H, brs), 6.83 (1H, s), 4.30-4.39 (2H, quart), 2.82-2.92 (1H, quin), 1.83-1.96 (2H, m), 1.57-1.83 (6H, 2×m), 1.33-1.40 (3H, t) ppm. LRMS (electrospray): m/z [M−H]+ 211.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06967204B2
출처 데이터셋uspto-grants-2005_11
ORD IDord-1201cb2fc16e4c0cb08428a9b1d66098
출처 메모uspto-grants-2005_11