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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 47672생성일: 2026년 10월 24일

Imidazole → tert-butyl(dimethyl)silyl [(2R)-6-iodo-3,4-dihydro-2H-chromen-2-yl]methyl ether

https://huagongshe.com/ko/reaction/47672

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참여 물질

역할이름HCID투입량
반응물ImidazoleHCID 795—
반응물WaterHCID 962—
반응물tert-Butyldimethylsilyl chlorideHCID 28928—
반응물[(2R)-6-iodo-3,4-dihydro-2H-chromen-2-yl]methanolHCID 9943850—
용매DimethylformamideHCID 6228—
생성물tert-butyl(dimethyl)silyl [(2R)-6-iodo-3,4-dihydro-2H-chromen-2-yl]methyl etherHCID 1027255279%

반응 조건

온도27 °C

반응 단계

A reaction mixture containing [(2R)-6-iodo-3,4-dihydro-2H-chromen-2-yl]methanol (Example 8, 5 g, 17.2 mmol, 1.0 eq), tert-butyldimethylsilyl chloride (20.6 mmol, 1.2 eq), and imidazole (43 mmol, 2.5 eq) in anhydrous DMF (35 mL) was stirred at 27° C. overnight. The resulting mixture was then cooled to room temperature, poured into water, and extracted with diethyl ether. The organic extract was washed with water, brine, dried over anhydrous sodium sulfate, concentrated, and purified by medium pressure column chromatography (Biotage 40S normal phase silica gel column, providing the product in 79% yield; M/z 405 [MH=].

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06699860B2
출처 데이터셋uspto-grants-2004_03
ORD IDord-e9250eeaa6ca4902be2256a984a0b951
출처 메모uspto-grants-2004_03