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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2259752생성일: 2026년 10월 24일

Dopac → 5-(2-Hydroxyethyl)-2-methyl-1,3-benzodioxole

https://huagongshe.com/ko/reaction/2259752

반응식

참여 물질

역할이름HCID투입량
반응물DopacHCID 547—
반응물Vinyl AcetateHCID 7904—
반응물Sodium HydroxideHCID 14798—
반응물Aluminium lithium hydrideHCID 21226445—
촉매Mercuric oxideHCID 30856—
용매WaterHCID 962—
용매TolueneHCID 1140—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물5-(2-Hydroxyethyl)-2-methyl-1,3-benzodioxoleHCID 1900162574.6%

반응 단계

A suspension of 1.0 g of 3,4-dihydroxyphenylacetic acid, 1.4 g of vinyl acetate, 6 mg of mercury oxide (yellow) and 0.03 ml of boron fluoride/ethyl etherate in 9 ml of toluene was stirred at room temperature for 14 h. The reaction mixture was diluted with ethyl acetate and washed with water and an aqueous common salt solution. The organic layer was dried over magnesium sulfate and the solvent was distilled off. An oil thus obtained was dissolved in 10 ml of tetrahydrofuran and the solution was added dropwise to a suspension of 0.5 g of lithium aluminum hydride in tetrahydrofuran under cooling with ice. The mixture was stirred at room temperature for 1 h. 0.5 ml of water, then 0.5 ml of a 15% aqueous sodium hydroxide solution and finally 1.5 ml of water were added thereto and an insoluble matter was filtered off. The filtrate was concentrated and treated according to silica gel column chromatography (ethyl acetate/hexane=1:1) to obtain 0.8 g of the intended compound in the form of a colorless oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05475024
출처 데이터셋uspto-grants-1995_12
ORD IDord-237408a16d374957be2a2740e478e8d8
출처 메모uspto-grants-1995_12