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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2,4,5-Trichlorophenol | HCID 7271 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2,5-Bis(ethylsulfonyl)pyridine | HCID 13278015 | — |
| Solvent | Sulfolane | HCID 31347 | — |
| Product | 5-(Ethylsulfonyl)-2-(2,4,5-trichlorophenoxy)pyridine | HCID 13102727 | 19.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04371537 |
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| Source dataset | uspto-grants-1983_02 |
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| ORD ID | ord-53c480b956914e26b5bad097cc994a91 |
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| Source note | uspto-grants-1983_02 |
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