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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 50125생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/50125

반응식

참여 물질

역할이름HCID투입량
반응물Methanesulfonic AcidHCID 6395—
반응물2,2,2-TrifluoroethanolHCID 6409—
반응물Tert-Butyl nitriteHCID 10906—
반응물Sulfuric acid magnesium salt (1:1)HCID 24083—
반응물2-Chloro-3-pyridylamineHCID 80528—
반응물Sodium BicarbonateHCID 516892—
생성물2-Chloro-3-(2,2,2-trifluoroethoxy)pyridineHCID 1205672870.1%

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), methanesulfonic acid (2.02 g, 21 mmol), and magnesium sulfate (3 g). 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 65° C. to 70° C. After cooling the solution it 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 (4.4 g) with an actual yield of 70.1%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06710180B2
출처 데이터셋uspto-grants-2004_03
ORD IDord-13c858555cab4c44b1e2deac7e473876
출처 메모uspto-grants-2004_03