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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 326366생성일: 2026년 10월 23일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물Methyl iodideHCID 6328—
반응물1,2-Ethanediamine, N1,N1,N2-trimethyl-HCID 67338—
반응물4-Phenyl-3-furaldehydeHCID 15037148—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
용매HexaneHCID 8058—
생성물2-Methyl-4-phenyl-3-furaldehydeHCID 15037159—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05268387
출처 데이터셋uspto-grants-1993_12
ORD IDord-4905bc23f6ca4ea7b240873898cccace
출처 메모uspto-grants-1993_12