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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2-(4-Hydroxy-phenoxy)-propionic acid | HCID 101182 | — |
| Reactant | 2,3-Difluoro-5-(trifluoromethyl)pyridine | HCID 13421547 | — |
| Solvent | Thionyl Chloride | HCID 24386 | — |
| Product | 4-((3-Fluoro-5-(trifluoromethyl)-2-pyridinyl)oxy)phenoxy propanoic acid | HCID 15592824 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04851539 |
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| Source dataset | uspto-grants-1989_07 |
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| ORD ID | ord-12d62d18bc2d4cfeb3209f6bfb785ee3 |
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| Source note | uspto-grants-1989_07 |
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