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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 341564Generated: October 25, 2026

2,2,2-Trifluoroethanol → 3-(2,2,2-Trifluoroethoxy)pyridine-2-carboxylic acid

https://huagongshe.com/reaction/341564

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,2,2-TrifluoroethanolHCID 6409—
Reactant3-Fluoropyridine-2-carboxylic acidHCID 2762786—
ReactantPotassium tert-butoxideHCID 23665647—
SolventWaterHCID 962—
Product3-(2,2,2-Trifluoroethoxy)pyridine-2-carboxylic acidHCID 5747587949%

Reaction Steps

Potassium tert-butoxide (954 mg, 8.51 mmol) was charged to a sealed tube with 2,2,2-trifluoroethanol (4 mL) and 3-fluoropyridine-2-carboxylic acid (400 mg, 2.84 mmol) and the mixture was heated to 130 C for 26 h, then to 150 C for 4 h, and then to 120 C for approximately 18 h. The mixture was diluted with water (6 mL) and washed with DCM (2×4 mL), which was then discarded. 1M HCl was added to bring the solution to pH 7 and the aqueous was extracted with DCM (2×4 mL). The extraction process was repeated as above at pH 5, 4 and 3. The combined organic extractions were dried over sodium sulfate and evaporated under vacuum to afford the title compound as a white solid (305 mg, 49%). Method B HPLC-MS: MH+ requires m/z=222. Found: m/z=222, Rt=0.73 min (100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08895733B2
Source datasetuspto-grants-2014_11
ORD IDord-2d9fe477dafa4577916b6fc50060584f
Source noteuspto-grants-2014_11