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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 50127생성일: 2026년 10월 23일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물Methanesulfonic AcidHCID 6395—
반응물2,2,2-TrifluoroethanolHCID 6409—
반응물Tert-Butyl nitriteHCID 10906—
반응물2-Chloro-3-pyridylamineHCID 80528—
반응물Sodium BicarbonateHCID 516892—
생성물2-Chloro-3-(2,2,2-trifluoroethoxy)pyridineHCID 1205672867.3%

반응 단계

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%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06710180B2
출처 데이터셋uspto-grants-2004_03
ORD IDord-178acea5fc59416fa07e80f9c264941c
출처 메모uspto-grants-2004_03