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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1488729Generated: October 26, 2026

Thiophenol → 2-chloro-6-thiophenylpyridine N-oxide

https://huagongshe.com/reaction/1488729

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThiophenolHCID 7969—
ReactantSodium HydroxideHCID 14798—
Reactant2,6-Dichloropyridine N-OxideHCID 817673—
SolventDimethyl SulfoxideHCID 679—
Product2-chloro-6-thiophenylpyridine N-oxideHCID 86748730—

Reaction Steps

The 1.64 g (0.010 moles) of 2,6-dichloropyridine N-oxide and 1.11 g (99%) (0.010 moles) of thiophenol was reacted with 0.400 g (0.010 moles) of ground sodium hydroxide of 16.4 ml of DMSO at 80° C. for 5 hours to give 2-chloro-6-thiophenylpyridine N-oxide. It was reacted with 1.20 g (0.030 moles) of ground sodium hydroxide at 80° C. for 2.5 hours to give 1-hydroxy-6-thiophenylpyridine-2(1H)-one. After cooling, it was added 148 ml of water and was adjusted with 6N HCl to pH 3. The precipitate was filtered, washed with water and washed with hexanes to give 1.64 g (75%). It was recrystallized from ethanol: mp 180°-181° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05675013
Source datasetuspto-grants-1997_10
ORD IDord-d3546c304ec74543916c2c1ae1a57f55
Source noteuspto-grants-1997_10