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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1401422Generated: October 29, 2026

Tetrahydrofuran → 3-(Oxiran-2-yl)pyridine

https://huagongshe.com/reaction/1401422

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
Reactant3-PyridinecarboxaldehydeHCID 10371—
ReactantSodium hydrideHCID 24758—
ReactantTrimethylsulfonium iodideHCID 75127—
SolventDimethyl SulfoxideHCID 679—
Product3-(Oxiran-2-yl)pyridineHCID 13319561—

Reaction Conditions

Temperature65 °C

Reaction Steps

Sodium hydride 50% dispersion in oil (1-1.8 equiv.) is taken in DMSO and heated at 65° C. for 1 h. THF is added to at the mixture at the same temperature and heated for 10 min. The reaction mixture is cooled to 0° C. and Trimethylsulfonium iodide (1-1.2 equiv.) is added, followed by nicotinaldehyde (1 equiv.) and the contents are stirred at RT for 1 h. The reaction is monitored by TLC and LCMS. After completion of the reaction, the reaction mixture is poured in ice and extracted with diethyl ether, dried over anhydrous sodium sulfate and evaporated under reduced pressure to afford crude product (3-(oxiran-2-yl)pyridine).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08907097B2
Source datasetuspto-grants-2014_12
ORD IDord-c6076aefe43d425f9c63c685a7f50c80
Source noteuspto-grants-2014_12