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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 50123Generated: October 25, 2026

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

https://huagongshe.com/reaction/50123

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,2,2-TrifluoroethanolHCID 6409—
ReactantTrifluoroacetic acidHCID 6422—
ReactantTert-Butyl nitriteHCID 10906—
ReactantSulfuric acid magnesium salt (1:1)HCID 24083—
Reactant2-Chloro-3-pyridylamineHCID 80528—
ReactantSodium BicarbonateHCID 516892—
Product2-Chloro-3-(2,2,2-trifluoroethoxy)pyridineHCID 12056728—

Reaction Conditions

Temperature15 °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 15° C. and magnesium sulfate (2.6 g) is charged to the vessel. The reagent t-butyl nitrite (2.51 g of a 96% solution, 23.4 mmol) is added drop-wise to the vessel while maintaining the temperature in the range 15° C. to 20° C. The solution is 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 (1.58 g, crude yield 35.6%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06710180B2
Source datasetuspto-grants-2004_03
ORD IDord-d39c4576ec454630a4218cea4eedd2cf
Source noteuspto-grants-2004_03