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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1758006Generated: October 31, 2026

2,4,5-Trichlorophenol → 5-(Ethylsulfonyl)-2-(2,4,5-trichlorophenoxy)pyridine

https://huagongshe.com/reaction/1758006

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,4,5-TrichlorophenolHCID 7271—
ReactantPotassium CarbonateHCID 11430—
ReactantSodium HydroxideHCID 14798—
Reactant2,5-Bis(ethylsulfonyl)pyridineHCID 13278015—
SolventSulfolaneHCID 31347—
Product5-(Ethylsulfonyl)-2-(2,4,5-trichlorophenoxy)pyridineHCID 1310272719.2%

Reaction Conditions

Temperature170 °C

Reaction Steps

In 70 ml of sulfolane were mixed 10.5 g of 2,5-bis(ethylsulfonyl)pyridine, 15.8 g of 2,4,5-trichlorophenol and 11.06 g of potassium carbonate. The mixture was warmed gradually to 170° C. and maintained at that temperature for 2 hrs. The reaction mixture was cooled and then poured into 300 g of ice containing 4 g of sodium hydroxide. The aqueous solution was extracted with ether. The organic layer was washed with water, dried over MgSO4 and concentrated. The product was purified using a Water's Prep LC 500 instrument with 10% ethyl acetate/90% hexane as eluent. Recrystallization from diethyl ether gave 2.8 g, (19% yield), of purified 5-(ethylsulfonyl)-2-(2,4,5-trichlorophenoxy)pyridine, m.p. 120°-122° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04371537
Source datasetuspto-grants-1983_02
ORD IDord-53c480b956914e26b5bad097cc994a91
Source noteuspto-grants-1983_02