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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 733181생성일: 2026년 10월 27일

2,2-Dimethyl-1,3-dioxane-4,6-dione → Ethyl 6-(benzyloxy)-3-oxohexanoate

https://huagongshe.com/reaction/733181

반응식

참여 물질

역할이름HCID투입량
반응물2,2-Dimethyl-1,3-dioxane-4,6-dioneHCID 16249—
반응물2-DimethylaminopyridineHCID 21885—
반응물Isopropenyl chloroformateHCID 93846—
반응물Potassium bisulfateHCID 516920—
반응물4-(Benzyloxy)butanoic acidHCID 562201—
용매DichloromethaneHCID 6344—
생성물Ethyl 6-(benzyloxy)-3-oxohexanoateHCID 10264779—

반응 조건

온도0 °C

반응 단계

4-Benzyloxybutyric acid (6.38 mL), Meldrum's acid (5.76 g) and dimethylaminopyridine (9.77 g) were dissolved in DCM (200 mL) and cooled to 0° C. A solution of isopropenyl chloroformate in dichloromethane (100 mL) was added dropwise and stirring at 0° C. continued for a further 2 h. Potassium hydrogen sulphate (200 mL of a 10% aqueous solution) was then added, the organic phase separated, dried over sodium sulphate, and evaporated under reduced pressure. The residue was dissolved in ethanol (200 mL) and heated at reflux overnight. Following cooling, the solvent was evaporated under reduced pressure and the resultant oil was purified by flash silica column chromatography. 6-Benzyloxy-3-oxo-hexanoic acid ethyl ester was isolated as an orange oil (8.53 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07589095B2
출처 데이터셋uspto-grants-2009_09
ORD IDord-89951e2fd3ce4e01a09824d7d1d6ead2
출처 메모uspto-grants-2009_09