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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1759935생성일: 2026년 10월 23일

Potassium Carbonate → 4-(2-Butynyloxy)-6-(2,6-dichloro-4-fluorophenoxy)pyrimidine

https://huagongshe.com/ko/reaction/1759935

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참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물Ammonium ChlorideHCID 25517—
반응물Phenol, 2,6-dichloro-4-fluoro-HCID 94950—
반응물4-(2-Butynyloxy)-6-chloropyrimidineHCID 12137602—
용매DimethylformamideHCID 6228—
생성물4-(2-Butynyloxy)-6-(2,6-dichloro-4-fluorophenoxy)pyrimidineHCID 2259982561.4%

반응 조건

온도80 °C

반응 단계

To 2 ml of N,N-dimethylformamide were added 0.2 g of 4-chloro-6-(2-butynyloxy)pyrimidine, 0.23 g of potassium carbonate, and 0.20 g of 2,6-dichloro-4-fluorophenol, followed by stirring at 80° C. for 7 hours. The reaction mixture was then left for cooling to room temperature and poured into a saturated aqueous ammonium chloride solution, which was extracted three times with chloroform. The chloroform layers were combined, washed with diluted hydrochloric acid and then with water, and dried over anhydrous magnesium sulfate and then concentrated. The residue was subjected to silica gel column chromatography to give 0.22 g of 4-(2-butynyloxy)-6-(2,6-dichloro-4-fluorophenoxy)pyrimidine (the present compound (160)).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06838463B2
출처 데이터셋uspto-grants-2005_01
ORD IDord-510097ca8d5b4f92b1b4b3e48fd49b98
출처 메모uspto-grants-2005_01