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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 47672Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/47672

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktImidazoleHCID 795—
EduktWaterHCID 962—
Edukttert-Butyldimethylsilyl chlorideHCID 28928—
Edukt[(2R)-6-iodo-3,4-dihydro-2H-chromen-2-yl]methanolHCID 9943850—
LösungsmittelDimethylformamideHCID 6228—
Produkttert-butyl(dimethyl)silyl [(2R)-6-iodo-3,4-dihydro-2H-chromen-2-yl]methyl etherHCID 1027255279%

Reaktionsbedingungen

Temperatur27 °C

Reaktionsschritte

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=].

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06699860B2
Quelldatensatzuspto-grants-2004_03
ORD IDord-e9250eeaa6ca4902be2256a984a0b951
Quellennotizuspto-grants-2004_03