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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1873405생성일: 2026년 10월 26일

Water → 2-(4-Propylphenyl)selenophene

https://huagongshe.com/reaction/1873405

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Sodium CarbonateHCID 10340—
반응물2-BromoselenopheneHCID 137013—
반응물(4-Propylphenyl)boronic acidHCID 4100861—
촉매HCID 178418397HCID 178418397—
용매Toluene ethanolHCID 21863594—
생성물2-(4-Propylphenyl)selenopheneHCID 59456318—

반응 단계

A mixture of 26.0 g (0.12 mol) of 2-bromoselenophene, 20.5 g (0.13 mol) of 4-propylphenylboronic acid, 7.0 g (6.1 mmol) of tetrakis-(triphenylphosphine)palladium(0) and 140 ml of 2 N sodium carbonate soln. in 300 ml of toluene/ethanol (1:1) is heated under reflux for 20 h. A further 7.0 g (6.06 mmol) of tetrakis(triphenylphosphine)palladium(0) are added, and the mixture is refluxed again for 3 h. After cooling, water is added, and the organic phase is separated off. The aqueous phase is extracted with toluene, and the combined organic phases are washed with water and sat. sodium chloride soln. The solution is dried using sodium sulfate and concentrated to dryness. The residue is purified by column chromatography (SiO2, n-heptane). 2-(4-Propylphenyl)selenophene is obtained as a yellow liquid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08304036B2
출처 데이터셋uspto-grants-2012_11
ORD IDord-a75389601c804176925a13fc513e3467
출처 메모uspto-grants-2012_11