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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1049589Erstellt: 27. Oktober 2026

Imidazole → 4-((Tert-butyl(dimethyl)silyl)oxy)-2'-fluoro-5'-methoxybiphenyl-2-yl trifluoromethanesulfonate

https://huagongshe.com/reaction/1049589

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktImidazoleHCID 795—
EduktAmmonium ChlorideHCID 25517—
Edukttert-Butyldimethylsilyl chlorideHCID 28928—
Edukt2'-Fluoro-4-hydroxy-5'-methoxybiphenyl-2-yl trifluoromethanesulfonateHCID 117760123—
LösungsmittelDimethylformamideHCID 6228—
Produkt4-((Tert-butyl(dimethyl)silyl)oxy)-2'-fluoro-5'-methoxybiphenyl-2-yl trifluoromethanesulfonateHCID 13173603380%

Reaktionsschritte

To a solution of 2′-fluoro-4-hydroxy-5′-methoxybiphenyl-2-yl trifluoromethanesulfonate (2.85 g) and imidazole (800 mg) in DMF (50 mL) was added tert-butyldimethylchlorosilane (1.42 g), and the mixture was stirred at room temperature for 1 hr. To the reaction mixture was added saturated aqueous ammonium chloride solution, and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine, and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography (ethyl acetate/hexane) to give the title compound (2.99 g) as a colorless oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09382188B2
Quelldatensatzuspto-grants-2016_07
ORD IDord-ccb2a4191dca44699145a6059d3a0472
Quellennotizuspto-grants-2016_07