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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1757996Generated: November 3, 2026

Water → 5-(Methylsulfonyl)-2-(4-((trifluoromethyl)thio)phenoxy)pyridine

https://huagongshe.com/reaction/1757996

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant4-(Trifluoromethylsulfanyl)phenolHCID 3815158—
Reactant2,5-Bis(methylsulfonyl)pyridineHCID 13102675—
ReactantPotassium tert-butoxideHCID 23665647—
SolventTetrahydrofuranHCID 8028—
Product5-(Methylsulfonyl)-2-(4-((trifluoromethyl)thio)phenoxy)pyridineHCID 1310269060%

Reaction Steps

To 4.95 g of 4-(trifluoromethylthio)phenol dissolved in a 20 ml THF/20 ml DMSO mixture was added 2.9 g of t-BuOK and then 6.0 g of 2,5-bis(methylsulfonyl) pyridine, and the resulting mixture heated at 58° C. for 11/2 hrs. The reaction mixture was cooled to room temperature and added to approximately 3 to 4 volumes of water. The yellow-brown precipitate that formed was removed by filtration and then recrystallized from CH2Cl2 /ethanol. The purified product, 5-(methylsulfonyl)-2-(4-((trifluoromethyl)thio)phenoxy)pyridine, (60% yield), was recovered as tiny cream-white plates, m.p. 134°-135° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04371537
Source datasetuspto-grants-1983_02
ORD IDord-a9cb7010e84a46f4a95b9632910e5774
Source noteuspto-grants-1983_02