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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 273950생성일: 2026년 10월 23일

Methyl iodide → 5Methyl-2-trimethylsilyl-4-furaldehyde

https://huagongshe.com/ko/reaction/273950

반응식

참여 물질

역할이름HCID투입량
반응물Methyl iodideHCID 6328—
반응물5-(Trimethylsilyl)furan-3-carbaldehydeHCID 15663251—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
용매HexaneHCID 8058—
생성물5Methyl-2-trimethylsilyl-4-furaldehydeHCID 15744590—

반응 단계

n-Butyl lithium (a 1.6M solution in hexane; 2.04 ml, 3.28 mmol) was added dropwise to a solution of N,N'N'-trimethylethylenediamine (0.46 ml, 3.56 mmol) in tetrahydrofuran (7 ml) at -78 degrees under argon. After 15 minutes, a solution of 2-trimethylsilyl-4-furaldehyde (0.5 g, 2.98 mmol) in tetrahydrofuran (2 ml) was added, followed by n-butyl lithium (3.72 ml, 5.94 mmol) after 15 minutes. Iodomethane (1.12 ml, 17.9 mmol) was then added and the mixture was allowed to warm to room temperature gradually over 1/2 hour. The mixture was quenched with brine and extracted with ethyl ether. Evaporation of the dried (magnesium sulphate) extracts gave an oil, which was purified by flash chromatography using 10% ethyl ether/hexane. Fractions with Rf of about 0.22 on evaporation afforded the title methylfuran as a light yellow oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05387606
출처 데이터셋uspto-grants-1995_02
ORD IDord-2fc87ac0d97f411c83c6462c5543ed1c
출처 메모uspto-grants-1995_02