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HRID 326366作成日:2026年10月24日

Methyl iodide → 2-Methyl-4-phenyl-3-furaldehyde

https://huagongshe.com/ja/reaction/326366

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl iodideHCID 6328—
反応物1,2-Ethanediamine, N1,N1,N2-trimethyl-HCID 67338—
反応物4-Phenyl-3-furaldehydeHCID 15037148—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
溶媒HexaneHCID 8058—
生成物2-Methyl-4-phenyl-3-furaldehydeHCID 15037159—

反応手順

n-Butyllithium (a 1.6m solution in hexane, 2.43 ml, 3.89 mmol) was added to a solution of trimethylethylenediamine (397 mg, 3.89 mmol) in tetrahydrofuran (25 ml) at 0 degrees under argon. After 20 minutes the solution was cooled to -78 degres and 4-phenyl-3-furaldehyde (608 mg, 3.35 mmol) was added. This mixture was allowed to gradually warm to -20 degrees and stirred for 11/2 hours, then recooled to -78 degrees before n-butyllithium (a 1.6M solution in hexane, 2.43 ml, 3.89 mmol) was added dropwise. The stirring mixture was again gradually warmed to -20 degrees and stirred for 2 hours before iodomethane (2.56 g 17.67 mmol) was added. After stirring for 18 hours at -20 degrees the reaction was quenched with ice-cold 10% (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 20% ethyl ether/hexanes to give the title aldehyde.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05268387
出典データセットuspto-grants-1993_12
ORD IDord-4905bc23f6ca4ea7b240873898cccace
出典メモuspto-grants-1993_12