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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 339662Generated: October 25, 2026

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

https://huagongshe.com/reaction/339662

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
Reactant8-Hydroxy-2-quinolinecarboxaldehydeHCID 599342—
SolventDichloromethaneHCID 6344—
Product8-(Tert-butyldimethylsilyloxy)quinoline-2-carbaldehydeHCID 5856708283%

Reaction Steps

8-Hydroxyquinoline-2-carbaldehyde (5.00 g, 28.9 mmol) and imidazole (4.32 g, 63.5 mmol) were dissolved in DCM (50 mL) under N2. The reaction mixture was cooled to 0° C. after which time tert-butylchlorodimethylsilane (4.94 g, 31.8 mmol) was added. After stirring for 16 hours at ambient temperature, the reaction mixture was partitioned between DCM and H2O. The organic layer was washed with H2O and aqueous saturated NaHCO3, dried over Na2SO4, filtered and concentrated under reduced pressure to afford an orange oil. The residue was purified via flash column chromatography (10:1 Hexane/EtOAc) to provide 6.85 g (83%) of desired product as a yellow/orange oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08895550B2
Source datasetuspto-grants-2014_11
ORD IDord-8b72e96bd29f41a38b067d733efbf1ca
Source noteuspto-grants-2014_11