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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1700335생성일: 2026년 10월 27일

Benzyl Alcohol → Benzyl 4,4-dimethoxy-3-oxobutyrate

https://huagongshe.com/reaction/1700335

반응식

참여 물질

역할이름HCID투입량
반응물Benzyl AlcoholHCID 244—
반응물PhosphateHCID 1061—
반응물Ethyl 4,4-dimethoxy-3-oxobutanoateHCID 248327—
촉매4-(Dimethylamino)pyridineHCID 14284—
용매TolueneHCID 1140—
생성물Benzyl 4,4-dimethoxy-3-oxobutyrateHCID 18318278—

반응 단계

2.68 g (14.1 mmol) of ethyl 4,4-dimethoxy-3-oxo-butyrate, 3.62 ml (34.9 mmol) of benzyl alcohol and 244 mg (2.0 mmol) of 4-dimethylaminopyridine were heated under reflux in 40 ml of toluene for three nights. A phosphate buffer solution was added to the obtained reaction solution. After the extraction with ethyl acetate, the organic layer was washed with a saturated aqueous salt solution and then dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure, and the residue was purified by the silica gel chromatography (hexane/ethyl acetate=9:1) to obtain the title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06350762B1
출처 데이터셋uspto-grants-2002_02
ORD IDord-5528c3d14ce94083a61c9fa6555a229c
출처 메모uspto-grants-2002_02