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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1041949Generated: October 29, 2026

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

https://huagongshe.com/reaction/1041949

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 numberUS08557809B2
Source datasetuspto-grants-2013_10
ORD IDord-a6238b8f1c684b87b03ba4e20cc0765c
Source noteuspto-grants-2013_10