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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1392861Generated: November 4, 2026

Pyridine → 2-tert-butyl-4-chloro-5-(2-p-toluenesulfonyloxy-1-(4-tert-butylphenyl)-1-ethyl)oxy-3(2H)-pyridazinone

https://huagongshe.com/reaction/1392861

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactanto-Toluenesulfonyl chlorideHCID 8623—
Reactant2-tert-butyl-4-chloro-5-(2-hydroxy-1-(4-tert-butylphenyl)-1-ethyl)oxy-3(2H)-pyridazinoneHCID 67100316—
SolventEthyl AcetateHCID 8857—
Product2-tert-butyl-4-chloro-5-(2-p-toluenesulfonyloxy-1-(4-tert-butylphenyl)-1-ethyl)oxy-3(2H)-pyridazinoneHCID 86600392—

Reaction Steps

To a 15 ml round bottom flask charged with 2-tert-butyl-4-chloro-5-(2-hydroxy-1-(4-tert-butylphenyl)-1-ethyl)oxy-3(2H)-pyridazinone (0.25 g, 0.66 mmol) is added pyridine. Toluenesulfonyl chloride (0.15 g, 0.79 mmol) is then added to it and the mixture stirred for 4 hours. The reaction mixture is diluted with ethyl acetate, washed with 5% copper sulfate solution and then with water and dried. After removing the solvent on the rotary evaporator the crude is purified by flash chromatography using ethyl acetate-hexanes as the eluting mixture.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07344702B2
Source datasetuspto-grants-2008_03
ORD IDord-5ef632fc54914083a8c8f2bc3634c703
Source noteuspto-grants-2008_03