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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1877195생성일: 2026년 10월 27일

1,2-Dimethoxyethane → (2-Methyl-5-{4-[3-(methylsulfanyl)propoxy]phenyl}furan-3-yl)methanol

https://huagongshe.com/reaction/1877195

반응식

참여 물질

역할이름HCID투입량
반응물1,2-DimethoxyethaneHCID 8071—
반응물Sodium CarbonateHCID 10340—
반응물Tert-butyl({5-[(5,5-dimethyl-1,3,2-dioxaborinan-2-yl)methyl]-2-methylfuran-3-yl}methoxy)dimethylsilaneHCID 68511011—
반응물1-Bromo-4-[3-(methylsulfanyl)propoxy]benzeneHCID 68511537—
촉매HCID 178418397HCID 178418397—
용매WaterHCID 962—
생성물(2-Methyl-5-{4-[3-(methylsulfanyl)propoxy]phenyl}furan-3-yl)methanolHCID 6850759288.4%

반응 단계

A mixture of tert-butyl({5-[(5,5-dimethyl-1,3,2-dioxaborinan-2-yl)methyl]-2-methylfuran-3-yl}methoxy)dimethylsilane (3.0 g), 1-bromo-4-[3-(methylsulfanyl)propoxy]benzene (2.8 g), tetrakis(triphenylphosphine)palladium(0) (0.5 g), 2N aqueous sodium carbonate solution (12 mL) and 1,2-dimethoxyethane (20 mL) was stirred overnight with refluxing under an argon atmosphere. The reaction mixture was poured into water, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, and dried over magnesium sulfate. The solvent was evaporated under reduced pressure. The residue was dissolved in tetrahydrofuran (20 mL), 1N tetrabutylammonium fluoride in tetrahydrofuran (10 mL) was added, and the mixture was stirred at room temperature for 2 hr. The reaction mixture was poured into water, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, and dried over magnesium sulfate. The solvent was evaporated under reduced pressure, purified by silica gel chromatography (0% ethyl acetate/hexane to 40% ethyl acetate/hexane), and crystallized from ethyl acetate/hexane to give the title compound (2.2 g, 84%) as a white crystal.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08309580B2
출처 데이터셋uspto-grants-2012_11
ORD IDord-9f411e3782e64de8882857efb7a9eb20
출처 메모uspto-grants-2012_11