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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 341524Generated: November 2, 2026

Hydrochloric Acid → 6-(2,2,2-Trifluoroethoxy)pyridine-3-carboxylic acid

https://huagongshe.com/reaction/341524

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant2,2,2-TrifluoroethanolHCID 6409—
ReactantPotassium HydroxideHCID 14797—
Reactant6-Chloronicotinic acidHCID 79222—
SolventDimethyl SulfoxideHCID 679—
Product6-(2,2,2-Trifluoroethoxy)pyridine-3-carboxylic acidHCID 278102882%

Reaction Steps

A mixture of 6-chloropyridine-3-carboxylic acid (6.0 g, 38.1 mmol), 2,2,2-trifluoroethanol (8.2 mL, 114.2 mmol) and potassium hydroxide (10.7 g, 190.4 mmol) in DMSO (50 mL) was stirred at 120 C for 18 h and left standing at room temperature for 2 days. A further 2 equivalents of potassium hydroxide and 1.5 equivalent of 2,2,2-trifluoroethanol were added and the reaction mixture was stirred at 120 C for 18 h. The mixture was acidified with a concentrated aqueous solution of HCl until a cream precipitate appeared. The precipitate was collected by filtration, washed with a 1N aqueous solution of HCl before being dissolved in EtOAc, washed 3 times with a 1N aqueous solution of HCl and 3 times with brine. The organic phase was dried over sodium sulfate, filtered and concentrated under vacuum to afford the title compound as a cream solid (6.9 g, 82%). Method C HPLC-MS: MH+ requires m/z=222 Found: m/z=222, Rt=1.24 min (98%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08895733B2
Source datasetuspto-grants-2014_11
ORD IDord-3acf4d7566d94215bb391f58f29d2d7f
Source noteuspto-grants-2014_11