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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 253702생성일: 2026년 10월 24일

Tripropylamine → 4-Chloro-6-methyl-2-(2-trifluoromethyl-phenyl)-pyrimidine

https://huagongshe.com/ko/reaction/253702

반응식

참여 물질

역할이름HCID투입량
반응물TripropylamineHCID 7616—
반응물Phosphorus oxychlorideHCID 24813—
반응물4(3H)-Pyrimidinone, 6-methyl-2-[2-(trifluoromethyl)phenyl]-HCID 135850835—
생성물4-Chloro-6-methyl-2-(2-trifluoromethyl-phenyl)-pyrimidineHCID 2193927184.1%

반응 조건

온도115 °C

반응 단계

A solution of 6-methyl-2-(2-trifluoromethyl-phenyl)-3H-pyrimidin-4-one (10.7 g, 41.9 mmol) in phosphorous oxychloride (39 mL, 419 mmol) was treated with tri-n-propylamine (16 mL, 83.9 mmol) and refluxed at 110-120° C. for 1 hours. The solvent was evaporated, azeotroped three times with toluene, then dried in vacuo. The residue was taken up in ethyl acetate, washed sequentially with 1 N sodium hydroxide, water and brine, then dried over sodium sulfate and concentrated. Purification by flash chromatography [SiO2, ethyl acetate:hexanes (1:9)] provided the title compound (9.61 g, 84% yield) as an orange oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07872129B2
출처 데이터셋uspto-grants-2011_01
ORD IDord-9bdff50eafca4cbbb0601d2dc0730ab9
출처 메모uspto-grants-2011_01