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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 232249Generated: October 28, 2026

Sodium Hydroxide → 4-((3-Fluoro-5-(trifluoromethyl)-2-pyridinyl)oxy)phenoxy propanoic acid

https://huagongshe.com/reaction/232249

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactant2-(4-Hydroxy-phenoxy)-propionic acidHCID 101182—
Reactant2,3-Difluoro-5-(trifluoromethyl)pyridineHCID 13421547—
SolventThionyl ChlorideHCID 24386—
Product4-((3-Fluoro-5-(trifluoromethyl)-2-pyridinyl)oxy)phenoxy propanoic acidHCID 15592824—

Reaction Conditions

Temperature115 °C

Reaction Steps

A fresh sample of 2-(4-((3-fluoro-5-(trifluoromethyl)-2-pyridinyl)oxy)phenoxy propanoic acid was prepared by the reaction of 2,3-difluoro-5-(trifluoromethyl)pyridine with 2-(4-hydroxyphenoxy)propanoic acid in the presence of 2 moles of sodium hydroxide as above described and 9.0 g (0.026 mole) was refluxed in excess SOCl2 for about 1/2 hour to prepare the corresponding acid chloride. The excess SOCl2 was removed by heating to 115° C. under an aspirator vacuum. The resulting acid chloride was added to a mixture of concentrated ammonium hydroxide (30 ml) and methanol (60 ml). The flask was rinsed with an additional 15 ml ammonium hydroxide mixed with about 25 ml of methanol and the two fractions were combined. The acid amide formed as a solid which was filtered out, rinsed with water, slurried in water, filtered, dried and analyzed. M.P. 140°-141° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04851539
Source datasetuspto-grants-1989_07
ORD IDord-12d62d18bc2d4cfeb3209f6bfb785ee3
Source noteuspto-grants-1989_07