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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 800생성일: 2026년 10월 23일

3-(Trifluoromethyl)phenol → 2-(Methylsulfanyl)-4-[3-(trifluoromethyl)phenoxy]pyrimidine

https://huagongshe.com/ko/reaction/800

반응식

참여 물질

역할이름HCID투입량
반응물3-(Trifluoromethyl)phenolHCID 7376—
반응물Sodium hydrideHCID 24758—
반응물4-Chloro-2-methylthiopyrimidineHCID 97113—
용매TetrahydrofuranHCID 8028—
생성물2-(Methylsulfanyl)-4-[3-(trifluoromethyl)phenoxy]pyrimidineHCID 19693871—

반응 단계

In THF, a phenoxide was prepared from 3-(trifluoromethyl)phenol (4.54 g, 0.0187×1.5 mol) was mixed with NaH (1.12 g (ca. 60% in mineral oil), 0.0187×1.5 mol), and 4-chloro-2-(methylthio)pyrimidine (Compound No. VII-1) (3.0 g, 0.0187 mol) was added thereto and the mixture was refluxed for about 10 hours. The reaction solution was partitioned between ethyl acetate and aqueous saturated sodium hydrogen carbonate to separate an organic phase. The organic phase was washed with aqueous saturated sodium chloride, dried over anhydrous sodium sulfate and concentrated, then recrystallized from a methanol/water system to obtain the intermediate compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05723412
출처 데이터셋uspto-grants-1998_03
ORD IDord-3d58caaef3e54ab9bff64df1e59b26f5
출처 메모uspto-grants-1998_03