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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2190756Generated: October 31, 2026

Ethanol → 2-(3-Ethoxypyridin-4-yl)-5-(trifluoromethyl)benzoxazole

https://huagongshe.com/reaction/2190756

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantPotassium CarbonateHCID 11430—
Reactant2-(3-Fluoropyridin-4-yl)-5-(trifluoromethyl)benzoxazoleHCID 66880180—
Product2-(3-Ethoxypyridin-4-yl)-5-(trifluoromethyl)benzoxazoleHCID 66880509—

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture of 0.28 g of 2-(3-fluoropyridin-4-yl)-5-(trifluoromethyl)benzoxazole, 0.27 g of potassium carbonate and 3 ml of ethanol was stirred while heating at 60° C. for two hours and then at 90° C. for 2.5 hours. The reaction mixture was cooled to room temperature, and then concentrated under reduced pressure. Water was added to the reaction mixture, followed by extraction with ethyl acetate twice. The combined organic layers were washed with a saturated sodium chloride solution, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was subjected to silica gel column chromatography to give 0.18 g of 2-(3-ethoxypyridin-4-yl)-5-(trifluoromethyl)benzoxazole (hereinafter, referred to as “active compound 69”).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08324387B2
Source datasetuspto-grants-2012_12
ORD IDord-24ae20dd77c04186b65c2cc9c28cd45c
Source noteuspto-grants-2012_12