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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 220489생성일: 2026년 10월 24일

Ethyl bromoacetate → Ethyl 4-oxo-3-propanoylhexanoate

https://huagongshe.com/ko/reaction/220489

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl bromoacetateHCID 7748—
반응물Sodium hydrideHCID 24758—
반응물3,5-HeptanedioneHCID 81923—
용매TetrahydrofuranHCID 8028—
생성물Ethyl 4-oxo-3-propanoylhexanoateHCID 5098800477%

반응 조건

온도0 °C

반응 단계

Dissolve heptane-3,5-dione (2.5 g, 19.5 mmol) in dry tetrahydrofuran (10 mL) and add the resulting solution dropwise to a chilled (0° C.) suspension of sodium hydride (0.94 g, 23.4 mmol, 60% dispersion in oil) in tetrahydrofuran (20 mL). Stir at 0° C. for 1 hr., then add bromoacetic acid ethyl ester (2.6 mL, 23.4 mmol) dropwise. Stir for 16 hr. at 0° C. and warm to room temperature. Partition the reaction mixture between diethyl ether (100 mL) and saturated aqueous ammonium chloride solution (50 mL). Separate the organic layer and wash with saturated aqueous sodium chloride solution (50 mL), dry (sodium sulfate), filter and concentrate. Purify using silica gel chromatography, eluting with 10:1 hexanes:ethyl acetate, to give 4-oxo-3-propionyl-hexanoic acid ethyl ester as an oil (3.2 g, 77%). 1H-NMR (400 MHz, CDCl3) δ 4.08 (m, 3H), 2.83 (d, 2H), 2.55 (q, 2H), 1.21 (t, 3H), 1.02 (t, 6H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08202873B2
출처 데이터셋uspto-grants-2012_06
ORD IDord-e5cf9ef8eeba4791a5c43d82a63ad79c
출처 메모uspto-grants-2012_06