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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 50124Generated: October 25, 2026

2,2,2-Trifluoroethanol → 2-Chloro-3-(2,2,2-trifluoroethoxy)pyridine

https://huagongshe.com/reaction/50124

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,2,2-TrifluoroethanolHCID 6409—
ReactantTrifluoroacetic acidHCID 6422—
ReactantTert-Butyl nitriteHCID 10906—
Reactant2-Chloro-3-pyridylamineHCID 80528—
ReactantSodium BicarbonateHCID 516892—
Product2-Chloro-3-(2,2,2-trifluoroethoxy)pyridineHCID 1205672862.6%

Reaction Conditions

Temperature55 °C

Reaction Steps

A reactor vessel is charged with 3-amino-2-chloropyridine (2.7 g, 21 mmol), 2,2,2-trifluoroethanol (15 g, 150 mmol), and trifluoroacetic acid (3.63 g, 31.8 mmol). The solution is cooled to the range 0° C. to 5° C. and then the reagent t-butyl nitrite (2.51 g of a 96% solution, 23.4 mmol) is added drop-wise to the vessel maintaining the temperature in the range 0° C. to 5° C. After stirring a few minutes the solution is transferred drop-wise to a reactor vessel containing 2,2,2-trifluoroethanol (20 g, 200 mmol) maintained at 55° C. The temperature rose to 70° C. during the drop-wise addition of the diazonium salt reaction mass. After cooling the solution, it neutralized with aqueous saturated sodium bicarbonate solution and then extracted with MTBE. The solvent is removed by evaporation to obtain 2-chloro-3-(2,2,2-trifluoroethoxy)pyridine as a crude oil (3.36 g) with an actual yield of 62.6%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06710180B2
Source datasetuspto-grants-2004_03
ORD IDord-6692566b87734cbdb07afed6ba1ac6e2
Source noteuspto-grants-2004_03