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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 586355Generated: October 26, 2026

m-Chloroperbenzoic acid → 4-(2-{[tert-Butyl(dimethyl)silyl]oxy}ethyl)-1-oxo-1lambda~5~-pyridine

https://huagongshe.com/reaction/586355

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
Reactant4-(Tert-butyldimethylsilyloxyethyl)-pyridineHCID 22321619—
SolventDichloromethaneHCID 6344—
Product4-(2-{[tert-Butyl(dimethyl)silyl]oxy}ethyl)-1-oxo-1lambda~5~-pyridineHCID 1975778983%

Reaction Steps

4-[2-(tert-Butyldimethylsilyloxy)ethyl]pyridine (15.2 g, 64 mmol) was dissolved in CH2Cl2 (200 mL). To this solution, m-chloroperbenzoic acid was added and the solution stirred at room temperature for 72 h. The solution was washed with aqueous NaOH (1 M) and layers separated. The water layer was extracted with CH2Cl2. The organic layers were combined, dried (K2CO3), filtered and concentrated under vacuum to provide 4-[2-(tert-butyldimethylsilyloxy)ethyl]pyridine-N-oxide (13.4 g, 83%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06936611B2
Source datasetuspto-grants-2005_08
ORD IDord-15282d92c34d4f75b636ffd906ba8871
Source noteuspto-grants-2005_08