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HRID 488237作成日:2026年10月23日

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

https://huagongshe.com/ja/reaction/488237

反応式

関与物質

役割名称HCID仕込み量
反応物ChlorotriethylsilaneHCID 13819—
反応物1-MethylpiperazineHCID 53167—
反応物4-Phenyl-3-furaldehydeHCID 15037148—
反応物ButyllithiumHCID 178418339—
反応物CID 53628100HCID 178418400—
溶媒TetrahydrofuranHCID 8028—
溶媒HexaneHCID 8058—
溶媒CyclohexaneHCID 8078—
生成物3-Phenyl-2-triethylsilyl-4furaldehydeHCID 15037149—

反応手順

n-Butyllithium (a 1.42 M 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 1.3 M solution 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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05298633
出典データセットuspto-grants-1994_03
ORD IDord-85a43c7db76f4054ac34b3386eef8203
出典メモuspto-grants-1994_03