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HRID 50127作成日:2026年10月24日

Methanesulfonic Acid → 2-Chloro-3-(2,2,2-trifluoroethoxy)pyridine

https://huagongshe.com/ja/reaction/50127

反応式

関与物質

役割名称HCID仕込み量
反応物Methanesulfonic AcidHCID 6395—
反応物2,2,2-TrifluoroethanolHCID 6409—
反応物Tert-Butyl nitriteHCID 10906—
反応物2-Chloro-3-pyridylamineHCID 80528—
反応物Sodium BicarbonateHCID 516892—
生成物2-Chloro-3-(2,2,2-trifluoroethoxy)pyridineHCID 1205672867.3%

反応手順

A reactor vessel is charged with 3-amino-2-chloropyridine (5.4 g, 42 mmol), 2,2,2-trifluoroethanol (50 g, 500 mmol), and methanesulfonic acid (4.1 g, 43 mmol). The solution is heated to the range 55° C. to 60° C. and then t-butyl nitrite (5.3 g of a 90% solution, 46 mmol) is added drop-wise to the vessel while maintaining the temperature at 60° C. to 65° C. After nitrogen evolution ceases, the solution is cooled, 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 (11.1 g) with an actual yield of 67.3%.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06710180B2
出典データセットuspto-grants-2004_03
ORD IDord-178acea5fc59416fa07e80f9c264941c
出典メモuspto-grants-2004_03