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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1745410생성일: 2026년 10월 26일

Ethyl oxoacetate → Ethyl 4-oxo-3,4-dihydro-2H-pyran-2-carboxylate

https://huagongshe.com/reaction/1745410

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl oxoacetateHCID 70211—
반응물1-Methoxy-3-trimethylsilyloxy-1,3-butadieneHCID 101051—
촉매ZincchlorideHCID 3007855—
용매BenzeneHCID 241—
생성물Ethyl 4-oxo-3,4-dihydro-2H-pyran-2-carboxylateHCID 2249509775%

반응 단계

A solution of glyoxylic acid ethyl ester, polymer form (2.02 g, 8.9 mmol) and (3-methoxy-1 methylene-allyloxy)trimethylsilane (1.9 ml, 8.9 mmol, Danishefsky's diene) in benzene (12 ml) was placed under nitrogen. Zinc chloride (0.5 N in tetrahydrofuran, 8.9 ml, 4.45 mmol) was added and the reaction stirred at ambient temperature for 72 hours. The mixture was concentrated in vacuo, diluted with ethyl acetate (100 ml) and washed with 1 N hydrochloric acid (20 ml), saturated sodium bicarbonate (20 ml), and brine (20 ml). The organic layer was dried (Na2SO4), filtered, and the solvent evaporated in vacuo. The residue was purified by silica gel chromatography using a mixture of ethyl acetate/hexane (1:2) as eluent. Pure fractions were collected and the solvent evaporated in vacuo which afforded 1.2 g (75%) of 4-oxo-3,4-dihydro-2H-pyran-2-carboxylic acid ethyl ester as an oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07019026B1
출처 데이터셋uspto-grants-2006_03
ORD IDord-92bd6faa833b4c6397d99a0800f07e7f
출처 메모uspto-grants-2006_03