돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1873409생성일: 2026년 10월 27일

Sodium Carbonate → 2-[4-(4-Ethylcyclohexyl)-2,3-difluorophenyl]selenophene

https://huagongshe.com/reaction/1873409

반응식

참여 물질

역할이름HCID투입량
반응물Sodium CarbonateHCID 10340—
반응물2-BromoselenopheneHCID 137013—
반응물4-(4-Ethylcyclohexyl)-2,3-difluorophenylboronic acidHCID 59456333—
촉매HCID 178418397HCID 178418397—
용매Toluene ethanolHCID 21863594—
생성물2-[4-(4-Ethylcyclohexyl)-2,3-difluorophenyl]selenopheneHCID 59456349—

반응 단계

A mixture of 8.9 g (42.4 mmol) of 2-bromoselenophene, 16.0 g (59.7 mmol) of 4-(4-ethylcyclohexyl)-2,3-difluorophenylboronic acid, 3.93 g (3.40 mmol) of tetrakis(triphenylphosphine)palladium(0) and 125 ml of 2 N sodium carbonate soln. in 600 ml of toluene/ethanol (1:1) is heated under reflux for 20 h. After cooling, the organic phase is separated off, and the aqueous phase is extracted with toluene. The combined organic phases are washed with sat. sodium chloride soln., and the solution is dried using sodium sulfate. The solution is concentrated to dryness, and the residue is purified by column chromatography (SiO2, toluene). The further purification is carried out by recrystallisation from n-heptane:EtOH=1:1 and IPA. 2-[4-(4-Ethylcyclohexyl)-2,3-difluorophenyl]selenophene is obtained as a pale-yellowish solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08304036B2
출처 데이터셋uspto-grants-2012_11
ORD IDord-9141115f49904b5e9db82f30946f0890
출처 메모uspto-grants-2012_11