Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1285090Generated: November 1, 2026

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

https://huagongshe.com/reaction/1285090

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 numberUS04565568
Source datasetuspto-grants-1986_01
ORD IDord-566780233640485f8f26780ae3b43549
Source noteuspto-grants-1986_01