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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 31685생성일: 2026년 10월 24일

Ethyl ketone → 4-((Benzyloxy)methyl)-2,2-diethyl-1,3-dioxolane

https://huagongshe.com/ko/reaction/31685

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl ketoneHCID 7288—
반응물3-(Benzyloxy)-1,2-propanediolHCID 98072—
반응물Sodium BicarbonateHCID 516892—
반응물p-Toluenesulfonic acid monohydrateHCID 521998—
용매TetrahydrofuranHCID 8028—
생성물4-((Benzyloxy)methyl)-2,2-diethyl-1,3-dioxolaneHCID 5979252767.1%

반응 단계

To a tetrahydrofuran (30 ml) solution of DL-α-O-benzyl glycerol (3 g, 16.5 mmol), 3-pentanone (17.5 ml, 165 mmol) and p-toluenesulfonic acid monohydrate (300 mg, 1.58 mmol) were added at room temperature and the mixture was stirred at the same temperature for 22 hours. To the reaction mixture, a saturated aqueous sodium hydrogen carbonate solution (5 ml) was added to adjust pH to about 8. The generated precipitate was removed by filtration and the filtrate was concentrated. The obtained residue was purified by silica gel column chromatography (NH silica gel, elution solvent: heptane/ethyl acetate=1/0 to 3/1 gradient). A desired fraction was concentrated to obtain the title compound (2.77 g, 67.1% yield) as a colorless oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07425634B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-b0ba235f52084fb9baa50225f74f6979
출처 메모uspto-grants-2008_09