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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1788084Generated: October 29, 2026

Toluene → Benzaldehyde, 4-[2-(5-ethyl-2-pyridinyl)ethoxy]-

https://huagongshe.com/reaction/1788084

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant5-Ethyl-2-pyridineethanolHCID 78894—
ProductBenzaldehyde, 4-[2-(5-ethyl-2-pyridinyl)ethoxy]-HCID 9881522—

Reaction Steps

10 g of 5-ethyl-2-pyridine ethanol, 10.2 ml triethylamine and 75 ml toluene are added to the round bottom assembly at ambient temperature. Thereafter 6.16 ml methane sulfonyl chloride are added via dropping funnel in 1 hour. The reaction mixture is stirred at ambient temperature for 1 hour and then washed with water. To the toluene layer are added 22.6 ml PEG200, 13.6 g potassium carbonate and 12 g 4-hydroxy benzaldehyde and the reaction mixture stirred for 4 hours at 80° C. The reaction mixture is cooled to ambient temperature and washed with 1 N alkali followed by water. Toluene is distilled off to obtain 4[2-(5-ethyl-2-pyridyl)ethoxy]benzaldehyde as oil to which are added methanol, pyrrolidine followed by 2,4-thiazolidinedione. The reaction mixture is stirred at 50° C. for 6 hours and then cooled to 10° C. Stirring is continued at 10° C. for 2 hours and the mixture filtered to obtain 5-[4[2-(5-ethyl-2-pyridinyl)ethoxy]phenyl]methenyl-2,4-thiazolidinedione. The wet cake is washed with Methanol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07511148B2
Source datasetuspto-grants-2009_03
ORD IDord-0dbd4d7198d1482db8cfa43ccca46c06
Source noteuspto-grants-2009_03