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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1880761Generated: November 1, 2026

Sodium Sulfite → 4-[2,2,2-trifluoro-1-(triethylsilyloxy)ethyl]pyridine N-oxide

https://huagongshe.com/reaction/1880761

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium SulfiteHCID 24437—
Reactantm-Chloroperbenzoic acidHCID 70297—
Reactant4-[2,2,2-Trifluoro-1-(triethylsilyloxy)ethyl]pyridineHCID 59570294—
SolventChloroformHCID 6212—
Product4-[2,2,2-trifluoro-1-(triethylsilyloxy)ethyl]pyridine N-oxideHCID 5957037886.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

To 40 ml of chloroform were added 5.5 g of 4-[2,2,2-trifluoro-1-(triethylsilyloxy)ethyl]pyridine, and 7.5 g of meta-chloroperbenzoic acid, and the mixture was stirred at 0° C. for 2 hours, and at room temperature for 3 hours. Thereafter, the reaction solution was poured into an aqueous saturated sodium sulfite solution, followed by extraction with chloroform three times. The organic layers were combined, washed with an aqueous saturated sodium chloride solution, dried with anhydrous magnesium sulfate, and concentrated. The residue was subjected to silica gel column chromatography to obtain 5 g of 4-[2,2,2-trifluoro-1-(triethylsilyloxy)ethyl]pyridine N-oxide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08318776B2
Source datasetuspto-grants-2012_11
ORD IDord-8472f885485a498c8d70d7349187b95d
Source noteuspto-grants-2012_11