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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 220456생성일: 2026년 10월 26일

Ethyl bromoacetate → Ethyl 3-acetyl-4-oxopentanoate

https://huagongshe.com/reaction/220456

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl bromoacetateHCID 7748—
반응물Sodium hydrideHCID 24758—
반응물AcetylacetoneHCID 31261—
용매TetrahydrofuranHCID 8028—
생성물Ethyl 3-acetyl-4-oxopentanoateHCID 8782094%

반응 단계

Add pentane-2,4-dione (2.0 g, 20.6 mmol) in tetrahydrofuran (30 mL) to a chilled (0° C.) suspension of 60% sodium hydride (0.99 g, 24.7 mmol) in tetrahydrofuran (40 mL). Stir for 1 hr. Then add bromoacetic acid ethyl ester (2.73 mL, 24.7 mmol) in tetrahydrofuran (30 mL) dropwise. Stir at 0° C. to room temperature for 16 hr. Partition between diethyl ether (100 mL) and saturated aqueous ammonium chloride solution (50 mL). Separate organic layer, dry (sodium sulfate), filter, concentrate and purify (silica gel chromatography, eluting with 9:1 hexanes:ethyl acetate), to give 3-acetyl-4-oxopentanoic acid ethyl ester (3.34 g, 94%). 1H NMR (CDCl3) δ 5.15 (q, 2H), 5.1 (t, 1H), 2.84 (d, 2H), 2.23 (s, 6H), 1.22 (t, 3H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08202873B2
출처 데이터셋uspto-grants-2012_06
ORD IDord-470d29832e0b4449b6e113eba46b2f63
출처 메모uspto-grants-2012_06