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HRID 1873397作成日:2026年10月27日

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

https://huagongshe.com/reaction/1873397

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium tert-butoxideHCID 23665647—
反応物5-(4-Ethoxy-2,3-difluorophenyl)selenophene-2-carbaldehydeHCID 59456315—
触媒Methyltriphenyliphosphonium bromideHCID 74505—
溶媒Hydrochloric AcidHCID 313—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
溶媒tert-Butyl methyl etherHCID 15413—
生成物2-(4-Ethoxy-2,3-difluorophenyl)-5-vinylselenopheneHCID 59456345—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08304036B2
出典データセットuspto-grants-2012_11
ORD IDord-fe73d39bd56242818070e29deecf8535
出典メモuspto-grants-2012_11