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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1871945Generated: November 2, 2026

2-Furanmethanethiol → 2,3-dimethyl-4-(2-furylmethylthio)pyridine N-oxide

https://huagongshe.com/reaction/1871945

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-FuranmethanethiolHCID 7363—
ReactantSodium hydrideHCID 24758—
Reactant4-Chloro-2,3-dimethyl-1-oxidopyridin-1-iumHCID 9877446—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
Product2,3-dimethyl-4-(2-furylmethylthio)pyridine N-oxideHCID 2246079480%

Reaction Steps

6 g (60% strength) of NaH are added in portions to 50 ml of dry dioxane, the mixture is stirred for 15 minutes, 11.7 g (0.11 mol) of 2-furylmethylmercaptan are metered in over a period of 20 minutes and the mixture is stirred again for 30 minutes until the evolution of gas has ended. A solution of 14.4 g (0.1 mol) of 4-chloro-2,3-dimethylpyridine N-oxide in 100 ml of dioxane is then added dropwise in the course of 20 minutes, and the reaction mixture is stirred at RT for 1 h, subsequently at 70° C. for 1 h and then at 100° C. for another 1 h. When the reaction has ended, the mixture is allowed to cool and is diluted with 500 ml of water and extracted 4 times with 300 ml of ethyl acetate each time. The combined organic phases are washed with water, dried over magnesium sulfate and concentrated and the residue is crystallized by addition of diisopropyl ether. 18.8 g (80% of theory) of 2,3-dimethyl-4-(2-furylmethylthio)-pyridine N-oxide of m.p. 111-112° C. are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06107312
Source datasetuspto-grants-2000_08
ORD IDord-ad9ee52462ea4d86beda4e513680fa83
Source noteuspto-grants-2000_08