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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 432083생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/432083

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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 번호US06660752B2
출처 데이터셋uspto-grants-2003_12
ORD IDord-7e3f16864e7948d4bc674023bef49cce
출처 메모uspto-grants-2003_12