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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1026539Generated: October 29, 2026

Trifluoroacetic acid → 2-[(2,5-Dichloropyridin-3-yl)oxy]-2-methylpropionic acid

https://huagongshe.com/reaction/1026539

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantTert-butyl 2-[(2,5-dichloropyridin-3-yl)oxy]-2-methylpropionateHCID 86671386—
SolventDichloromethaneHCID 6344—
Product2-[(2,5-Dichloropyridin-3-yl)oxy]-2-methylpropionic acidHCID 86671387125.5%

Reaction Steps

To a dichloromethane solution (157 ml) of tert-butyl 2-[(2,5-dichloropyridin-3-yl)oxy]-2-methylpropionate (79.1 g) was added at 0° C. trifluoroacetic acid (157 ml). The reaction solution was brought back to room temperature, stirred overnight, and then concentrated under reduced pressure. The residue was dissolved in ethyl acetate, washed sequentially with water and saturated sodium chloride solution, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was azeotroped with toluene to afford 2-[(2,5-dichloropyridin-3-yl)oxy]-2-methylpropionic acid (81.1 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08729095B2
Source datasetuspto-grants-2014_05
ORD IDord-0b56ff09ed5144dda50816a792bad4d0
Source noteuspto-grants-2014_05