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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2035567Generated: October 30, 2026

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

https://huagongshe.com/reaction/2035567

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 Conditions

Temperature0 °C

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., followed by addition of tert-butylchlorodimethylsilane (4.94 g, 31.8 mmol). 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 by flash column chromatography (10:1 Hexanes/EtOAc) to provide 6.85 g (83%) of desired product as a yellow/orange oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08575145B2
Source datasetuspto-grants-2013_11
ORD IDord-38943a566f824af98ca78e156361974e
Source noteuspto-grants-2013_11