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HRID 326370생성일: 2026년 10월 24일

Chlorotriethylsilane → 3-Phenyl-2-triethylsilyl-4furaldehyde

https://huagongshe.com/ko/reaction/326370

반응식

참여 물질

역할이름HCID투입량
반응물ChlorotriethylsilaneHCID 13819—
반응물1-MethylpiperazineHCID 53167—
반응물4-Phenyl-3-furaldehydeHCID 15037148—
반응물ButyllithiumHCID 178418339—
반응물CID 53628100HCID 178418400—
용매TetrahydrofuranHCID 8028—
용매HexaneHCID 8058—
용매CyclohexaneHCID 8078—
생성물3-Phenyl-2-triethylsilyl-4furaldehydeHCID 15037149—

반응 단계

n-Butyllithium (a 1.42M solution in hexane, 2.33 ml, 3.31 mmol) was added to a solution of 1-methylpiperazine (331 mg. 3.31 mmol) in tetrahydrofuran (15 ml) at 0 degrees under argon. After 15 minutes the solution was cooled to -78 degrees and 4-phenyl-3-furaldehyde (517 mg, 3.01 mmol) was added. This mixture was warmed to 0 degrees and stirred for 15 minutes, then recooled to -78 degrees before sec-butyllithium (a 1.3M solutin in cyclohexane, 2.77 ml, 3.61 mmol) was added dropwise. This solution was stirred 12 hours at -78 degrees C. before chlorotriethylsilane (1.81 g, 12.02 mmol) was added. The mixture was allowed to warm gradually to room temperature and stirred an additional 11/2 hours. The reaction was quenched with ice-cold 5% (V/V) hydrochloric acid and the organics were extracted into ethyl ether. The combined fractions were washed with saturated sodium bicarbonate, H2O and brine. Evaporation of the dried (magnesium sulfate) extracts gave an oil which was purified by flash chromatography on silica using 10% ethyl acetate/hexanes to give the title aldehyde.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05268387
출처 데이터셋uspto-grants-1993_12
ORD IDord-06cb8fb4f0194f48826c2847942f6dde
출처 메모uspto-grants-1993_12