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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1941815Generated: October 29, 2026

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

https://huagongshe.com/reaction/1941815

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2,2,3,3-Tetrafluoropropyl trifluoromethanesulfonateHCID 3792475—
ReactantMethyl 5-hydroxypyridine-2-carboxylateHCID 4715126—
SolventAcetoneHCID 180—
SolventDiethyl EtherHCID 3283—
Product5-(2,2,3,3-Tetrafluoro-propoxy)-pyridine-2-carboxylic acid methyl esterHCID 57475874—

Reaction Steps

A solution of 5-hydroxy-pyridine-2-carboxylic acid methyl ester (2.0 g, 13.1 mmol) in acetone (40 ml) was treated with potassium carbonate (5.415 g, 39.2 mmol) and trifluoro-methanesulphonic acid 2,2,3,3-tetrafluoropropyl ester. After 4 hours stirring at room temperature the suspension was diluted with diethylether. After filtration the solution was evaporated and the yellow solid purified by chromatography on silica gel using a gradient of heptane/ethyl acetate=100:0 to 30:70 as the eluent. The 5-(2,2,3,3-tetrafluoro-propoxy)-pyridine-2-carboxylic acid methyl ester was obtained as a light yellow solid (3.49 g, 76% of theory). MS (ISP): m/z=468.1 [M+H]+. b) 5-(2,2,3,3-Tetrafluoro-propoxy)-pyridine-2-carboxylic acid In a manner analogous to that described in example 29b), the hydrolysis of the 5-(2,2,3,3-tetrafluoro-propoxy)-pyridine-2-carboxylic acid methyl ester with lithium hydroxide yielded the title compound as a light yellow solid (yield 94% of theory). MS (ISP): m/z=253 [M]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08389513B2
Source datasetuspto-grants-2013_03
ORD IDord-2b072842f0ac414a84bc6fb95b231726
Source noteuspto-grants-2013_03