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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 571746Generated: October 27, 2026

Potassium Carbonate → 5-(2,2,3,3-Tetrafluoro-propoxy)-pyridine-2-carboxylic acid methyl ester

https://huagongshe.com/reaction/571746

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2,2,3,3-Tetrafluoropropyl trifluoromethanesulfonateHCID 3792475—
ReactantMethyl 5-hydroxypyridine-2-carboxylateHCID 4715126—
SolventAcetoneHCID 180—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
SolventAmmonium ChlorideHCID 25517—
Product5-(2,2,3,3-Tetrafluoro-propoxy)-pyridine-2-carboxylic acid methyl esterHCID 5747587466.4%

Reaction Steps

Methyl 5-hydroxypyridine-2-carboxylate (0.903 g, 5.90 mmol) is suspended in acetone (7 mL) and DMF (7 mL). 325 Mesh potassium carbonate (2.44 g, 17.69 mmol) is added in one portion and stirred at room temperature for 1.5 hours under nitrogen. 2,2,3,3-Tetrafluoropropyl trifluoromethanesulfonate (2.02 g, 7.67 mmol) is added drop wise and the mixture is stirred for 2 hours. The reaction mixture is diluted with ethyl acetate and saturated NH4Cl and extracted with ethyl acetate (3 times). The combined organic extracts are washed with brine, dried over Na2SO4, filtered, and the solvent removed in vacuo. The crude product is purified by silica gel flash chromatography, eluting with a gradient of 0-20% ethyl acetate in dichloromethane to give the title compound (1.047 g, 66%). ES/MS (m/e): 268.0 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09029367B2
Source datasetuspto-grants-2015_05
ORD IDord-e7b7d3f57c994e77bffbdf69ab6bebb9
Source noteuspto-grants-2015_05