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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2816생성일: 2026년 10월 23일

Chlorotrimethylsilane → 1-(2,5-Dimethyl-3-furyl)-1-(4-methyl-5-thiazolyl)ethanol

https://huagongshe.com/ko/reaction/2816

반응식

참여 물질

역할이름HCID투입량
반응물ChlorotrimethylsilaneHCID 6397—
반응물4-MethylthiazoleHCID 12748—
반응물3-Acetyl-2,5-dimethylfuranHCID 61527—
반응물Sodium BicarbonateHCID 516892—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
생성물1-(2,5-Dimethyl-3-furyl)-1-(4-methyl-5-thiazolyl)ethanolHCID 18936289—

반응 조건

온도-70 °C

반응 단계

4-Methylthiazole (6.51 g) in dry tetrahydrofuran (50 ml) was stirred under an atmosphere of dry nitrogen and cooled to -70° C. and n-butyllithium (2.5M solution in hexane, 29 ml) was added dropwise. After 30 minutes trimethylsilylchloride (7.14 g) was added and the mixture was allowed to warm to room temperature. After 30 minutes the mixture was again cooled to -70° C. and n-butyllithium (2.5M solution in hexane, 29 ml) was added dropwise. After 30 minutes 3-acetyl-2,5-dimethylfuran (10 g) was added dropwise. The mixture was stirred at -70° C. for 1 hour and was then allowed to warm to room temperature. After 30 minutes, aqueous sodium hydrogen carbonate was added and the mixture was extracted with diethylether. The combined extracts were washed, dried and evaporated to give the title compound which was recrystallised from diethylether. M.p. 100.5°-101.5° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05731335
출처 데이터셋uspto-grants-1998_03
ORD IDord-01df543a66bb4268b36a7edbe14246e3
출처 메모uspto-grants-1998_03