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HRID 47672作成日:2026年10月24日

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

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

反応式

関与物質

役割名称HCID仕込み量
反応物ImidazoleHCID 795—
反応物WaterHCID 962—
反応物tert-Butyldimethylsilyl chlorideHCID 28928—
反応物[(2R)-6-iodo-3,4-dihydro-2H-chromen-2-yl]methanolHCID 9943850—
溶媒DimethylformamideHCID 6228—
生成物tert-butyl(dimethyl)silyl [(2R)-6-iodo-3,4-dihydro-2H-chromen-2-yl]methyl etherHCID 1027255279%

反応条件

温度27 °C

反応手順

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=].

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06699860B2
出典データセットuspto-grants-2004_03
ORD IDord-e9250eeaa6ca4902be2256a984a0b951
出典メモuspto-grants-2004_03