Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 876383Erstellt: 26. Oktober 2026

Imidazole → 8-(Tert-butyldimethylsilyloxy)quinoline-2-carbaldehyde

https://huagongshe.com/reaction/876383

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktImidazoleHCID 795—
Edukttert-Butyldimethylsilyl chlorideHCID 28928—
Edukt8-Hydroxy-2-quinolinecarboxaldehydeHCID 599342—
LösungsmittelDichloromethaneHCID 6344—
Produkt8-(Tert-butyldimethylsilyloxy)quinoline-2-carbaldehydeHCID 5856708295,2%

Reaktionsschritte

To a solution of 8-hydroxyquinoline-2-carbaldehyde (15.0 g, 86.62 mmol) and imidazole (12.97 g, 190.6 mmol) in anhydrous CH2Cl2 (250 mL) at 0° C. was added tert-butylchlorodimethylsilane (14.36 g, 95.28 mmol). The mixture was allowed to warm slowly to ambient temperature over 16 hours and then partitioned between CH2Cl2 and water. The aqueous phase was extracted with CH2Cl2 and the combined organic phases were washed successively with saturated NaHCO3, water and brine, dried over Na2SO4, filtered and concentrated under reduced pressure. The residue was purified by silica gel pad filtration eluting with hexanes followed by 19:1 ethyl acetate/hexanes to provide 23.69 g (95%) of desired product as a dark yellow oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08987251B2
Quelldatensatzuspto-grants-2015_03
ORD IDord-dce37435330049cb8a94a5fc1ae3ea15
Quellennotizuspto-grants-2015_03