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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 845566Generated: October 31, 2026

4-Fluorophenol → HCID 20131576, compound

https://huagongshe.com/reaction/845566

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-FluorophenolHCID 9732—
ReactantPotassiumHCID 5462222—
ReactantHCID 20131574HCID 20131574—
SolventDiglymeHCID 8150—
ProductHCID 20131576HCID 2013157649.1%

Reaction Steps

3.0 g of 2-tert.-butyl-2-[(1H-1,2,4-triazol-1-yl)fluoromethyl]-oxirane, 1.7 g of 4-fluorophenol and 0.3 g of potassium p-fluorophenate in 10 ml of diethylene glycol dimethyl ether are stirred at 140° C. for 5 hours. After cooling, the mixture is taken up in ice water and extracted with ethyl acetate. The combined organic phases are washed with water, saturated sodium chloride solution and 2N sodium hydroxide solution and again with saturated sodium chloride solution, dried over sodium sulfate and evaporated. Crystallisation from a 1:4 ether/hexane mixture gives 2.3 g of 1-(4-fluorophenoxy)-2-tert.-butyl-2-hydroxy-3-fluoro-3-(1H-1,2,4-triazol-1-yl)-propane, melting point 89°-90° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04758670
Source datasetuspto-grants-1988_07
ORD IDord-0cf6473708a64ccd8605cb6c182a5003
Source noteuspto-grants-1988_07