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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1913672Generated: October 31, 2026

2-Methoxyethanol → 2-[3-(2-Methoxyethoxy)pyridin-4-yl]-5-(trifluoromethyl)benzoxazole

https://huagongshe.com/reaction/1913672

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-MethoxyethanolHCID 8019—
ReactantPotassium CarbonateHCID 11430—
Reactant2-(3-Fluoropyridin-4-yl)-5-(trifluoromethyl)benzoxazoleHCID 66880180—
SolventWaterHCID 962—
Product2-[3-(2-Methoxyethoxy)pyridin-4-yl]-5-(trifluoromethyl)benzoxazoleHCID 66880622—

Reaction Conditions

Temperature80 °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 2-methoxyethanol was stirred while heating at 80° C. for 2.5 hours. The reaction mixture was cooled to room temperature, and then 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 0.23 g of 2-[3-(2-methoxyethoxy)pyridin-4-yl]-5-(trifluoromethyl)benzoxazole (hereinafter, referred to as “active compound 120”).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08609705B2
Source datasetuspto-grants-2013_12
ORD IDord-e0b16ebf3a08470c9fa608b5020ccc23
Source noteuspto-grants-2013_12