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HRID 50124생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/50124

반응식

참여 물질

역할이름HCID투입량
반응물2,2,2-TrifluoroethanolHCID 6409—
반응물Trifluoroacetic acidHCID 6422—
반응물Tert-Butyl nitriteHCID 10906—
반응물2-Chloro-3-pyridylamineHCID 80528—
반응물Sodium BicarbonateHCID 516892—
생성물2-Chloro-3-(2,2,2-trifluoroethoxy)pyridineHCID 1205672862.6%

반응 조건

온도55 °C

반응 단계

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%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06710180B2
출처 데이터셋uspto-grants-2004_03
ORD IDord-6692566b87734cbdb07afed6ba1ac6e2
출처 메모uspto-grants-2004_03