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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 3916생성일: 2026년 10월 23일

2,2,2-Trifluoroethanol → 2-Amino-4-chloromethyl-6-(2,2,2-trifluoroethoxy)pyrimidine

https://huagongshe.com/ko/reaction/3916

반응식

참여 물질

역할이름HCID투입량
반응물2,2,2-TrifluoroethanolHCID 6409—
반응물SodiumHCID 5360545—
반응물4-Chloro-6-(chloromethyl)pyrimidin-2-amineHCID 20153488—
생성물2-Amino-4-chloromethyl-6-(2,2,2-trifluoroethoxy)pyrimidineHCID 20153493—

반응 단계

0.23 Parts of sodium metal was added to 10 parts of 2,2,2-trifluoroethanol with stirring and ice-bath cooling. The mixture was then stirred for several hours at room temperature until the sodium dissolved. This solution was added dropwise, over 30 minutes, to a stirred suspension of 1.78 parts of 2-amino-4-chloro-6-chloromethyl-pyrimidine in 25 parts of 2,2,2-trifluoro-ethanol and the resulting mixture was stirred at 60° C. for 18 hours. A further 0.1 parts of sodium was dissolved in 10 parts of 2,2,2-trifluoroethanol and added to the reaction mixture. Stirring at 60° C. was continued for a further 24 hours then the reaction mixture was cooled and evaporated in vacuo. The residue was partitioned between ethyl acetate and water. The organic layer was separated, washed with water, dried (MgSO4) and evaporated. The crude product was purified by chromatography on silica (Merck Kieselgel 60 using a 50:50 mixture of ether and 40°-60° petroleum ether as eluent followed by recrystallisation from a mixture of 60°-80° petroleum ether and ethyl acetate to give 2-amino-4-chloromethyl-6-(2,2,2-trifluoroethoxy)pyrimidine m.p. 77°-78° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04723006
출처 데이터셋uspto-grants-1988_02
ORD IDord-bf45258a6b514b10a95b14738e45793c
출처 메모uspto-grants-1988_02