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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2405645생성일: 2026년 10월 26일

Imidazole → Tert-butyldimethyl(4-((trimethylsilyl)ethynyl)benzyloxy)silane

https://huagongshe.com/reaction/2405645

반응식

참여 물질

역할이름HCID투입량
반응물ImidazoleHCID 795—
반응물Sulfuric acid magnesium salt (1:1)HCID 24083—
반응물tert-Butyldimethylsilyl chlorideHCID 28928—
반응물4-(Trimethylsilylethynyl)benzyl alcoholHCID 11241165—
용매TetrahydrofuranHCID 8028—
생성물Tert-butyldimethyl(4-((trimethylsilyl)ethynyl)benzyloxy)silaneHCID 5941715295.2%

반응 조건

온도0 °C

반응 단계

Under argon condition, (4-((trimethylsilyl)ethynyl)phenyl) methanol (258 mg, 1.26 mmol) was dissolved in 5 mL of dry THF and then cooled to 0° C., and imidazole (103 mg, 1.52 mmol) and TBSCl (228 mg, 1.52 mmol) dissolved in 3 mL of dry THF were added thereto. Thereafter, the temperature was raised to room temperature, and the reaction mixture was stirred for 15 hours at room temperature. Upon completion of the reaction, the reaction was terminated by adding 10 mL of aqueous saturated ammonium chloride solution. The reaction mixture was extracted with ethyl acetate (10 mL×4), and the organic layer thus obtained was treated with anhydrous magnesium sulfate to remove water. The precipitate was filtered out and the resulting solution was concentrated by distillation under reduced pressure, and purified by column chromatography to obtain 383 mg (1.20 mmol, 95%) of the desired compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08809012B2
출처 데이터셋uspto-grants-2014_08
ORD IDord-0f081623c6de4112b4767f864969c0ef
출처 메모uspto-grants-2014_08