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HRID 1873397생성일: 2026년 10월 26일

Potassium tert-butoxide → 2-(4-Ethoxy-2,3-difluorophenyl)-5-vinylselenophene

https://huagongshe.com/reaction/1873397

반응식

참여 물질

역할이름HCID투입량
반응물Potassium tert-butoxideHCID 23665647—
반응물5-(4-Ethoxy-2,3-difluorophenyl)selenophene-2-carbaldehydeHCID 59456315—
촉매Methyltriphenyliphosphonium bromideHCID 74505—
용매Hydrochloric AcidHCID 313—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
용매tert-Butyl methyl etherHCID 15413—
생성물2-(4-Ethoxy-2,3-difluorophenyl)-5-vinylselenopheneHCID 59456345—

반응 단계

3.0 g (8.4 mmol) of methyltriphenylphosphonium bromide are initially introduced in 50 ml of THF at 0° C., and 0.89 g (7.9 mmol) of potassium tertbutoxide is dissolved in 7 ml of THF is added. After 1.5 h at RT, 2.0 g (6.4 mmol) of 5-(4-ethoxy-2,3-difluorophenyl)selenophene-2-carbaldehyde are added, and the batch is stirred for 2.5 h. The mixture is diluted with MTBE, and water and 2 N hydrochloric acid are added. The organic phase is separated off, and the aqueous phase is extracted with MTBE. The combined organic phases are washed with sat. sodium chloride soln. and dried using sodium sulfate. The solution is concentrated to dryness, and the residue is purified by column chromatography (SiO2, n-heptane:EtOAc=10:1→5:1). Further purification is carried out by recrystallisation from n-heptane; 2-(4-ethoxy-2,3-difluorophenyl)-5-vinylselenophene is obtained as a yellow-orange solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08304036B2
출처 데이터셋uspto-grants-2012_11
ORD IDord-fe73d39bd56242818070e29deecf8535
출처 메모uspto-grants-2012_11