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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1013712Generated: October 31, 2026

m-Chloroperbenzoic acid → 2-(Trimethylsilyl)furo[3,2-B]pyridine 4-oxide

https://huagongshe.com/reaction/1013712

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
Reactant2-(Trimethylsilyl)furo[3,2-b]pyridineHCID 13636539—
SolventDichloromethaneHCID 6344—
Product2-(Trimethylsilyl)furo[3,2-B]pyridine 4-oxideHCID 66779372—

Reaction Steps

2-(Trimethylsilyl)furo[3,2-b]pyridine (14.68 g, 76.7 mmol) was dissolved in 80 mL DCM and cooled to 0° C. m-CPBA (33.1 g, 192 mmol) was dissolved in 160 mL DCM and slowly added to the reaction vessel. Upon complete addition, the reaction was warmed to RT and stirred for three hours. Reaction was diluted with DCM and washed twice with saturated sodium bicarbonate solution. 30 g of carbonate scavenger beads (—30 mmol) were added to the organic layer and the solution was stirred for 30 minutes. The reaction was filtered, washed with brine, dried with sodium sulfate, filtered, and concentrated. The material was purified via column chromatography (gradient elution 0-10% MeOH:DCM) to afford 2-(trimethylsilyl)furo[3,2-b]pyridine N-oxide as a light brown oil that solidified under high vacuum. MS: M+H+=208.2

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07981891B2
Source datasetuspto-grants-2011_07
ORD IDord-eb28cda1fb134e6f86efedc4147e041e
Source noteuspto-grants-2011_07