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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1815121생성일: 2026년 10월 25일

Ethyl 2-chloroacetoacetate → HCID 22499791, 화합물

https://huagongshe.com/reaction/1815121

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl 2-chloroacetoacetateHCID 11858—
반응물Sodium hydrideHCID 24758—
반응물1-Cyclopentyl-pent-4-yn-1-oneHCID 22499799—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
생성물HCID 22499791HCID 2249979176.3%

반응 조건

온도-40 °C

반응 단계

To a slurry of sodium hydride (480 mg, 60% suspension in mineral oil, 12 mmol) in THF (30 mL) cooled to −10° C. was added ethyl-2-chloroacetoacetate (1.66 mL, 12 mmol). The reaction was stirred until all gas evolution ceased. The reaction was then cooled to −40 ° C. and a solution of butyl lithium (4.8 mL, 2.5 M in ether, 12 mmol) was added. The reaction was stirred for 10 minutes, and then 1-cyclopentyl-pent-4-yn-1-one (0.60 g, 4 mmol) was added as a solution in THF (10 mL). The reaction was stirred for 1 hour, and then quenched with 40 mL saturated ammonium chloride. The solution was acidified further with 5 mL of 6 N HCl. The layers were separated, and the aqueous was extracted with ethyl acetate. The organics were combined and washed with water and then saturated sodium chloride. The organic phase was dried over sodium sulfate, filtered, and then concentrated. The crude product was then dissolved in toluene (13 mL) and bis(dibutylchlorotin) (1.027 g) was added. The solution was heated to reflux for one hour. The reaction was then concentrated and chromatographed (40 g silica gel, 2% MeOH in CH2Cl2) to yield the title compound (0.820 g, 76%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06878727B2
출처 데이터셋uspto-grants-2005_04
ORD IDord-6b7831eb8f16419eafb2d5c1349f0d51
출처 메모uspto-grants-2005_04