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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1193922생성일: 2026년 10월 27일

Hydrochloric Acid → 3-(4-chloro-2-fluoro-5-isopropoxyphenyl)-6-trifluoromethyl-2,4(1H,3H)-pyrimidinedione

https://huagongshe.com/reaction/1193922

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Sodium hydrideHCID 24758—
반응물Ethyl 3-amino-4,4,4-trifluorocrotonateHCID 5702529—
반응물4-Chloro-2-fluoro-5-isopropoxyphenyl isocyanateHCID 13272924—
용매WaterHCID 962—
용매TolueneHCID 1140—
용매DimethylformamideHCID 6228—
생성물3-(4-chloro-2-fluoro-5-isopropoxyphenyl)-6-trifluoromethyl-2,4(1H,3H)-pyrimidinedioneHCID 11428577—

반응 조건

온도0 °C

반응 단계

A solution of 1.0 g of ethyl 3-amino-4,4,4-trifluorocrotonate in 10 ml of absolute toluene is added dropwise while stirring at 0° C. during 15 minutes to a suspension of 0.24 g of a 55% sodium hydride dispersion in 20 ml of absolute dimethylformamide and the mixture is stirred at 0° C. for 15 minutes. The reaction mixture is subsequently cooled to -30° C. and treated with a solution of 1.26 g of 4-chloro-2-fluoro-5-isopropoxyphenyl isocyanate in 10 ml of absolute toluene. The temperature rises rapidly to -10° C. and the reaction mixture is thereafter stirred at room temperature for 2 hours. The reaction mixture is poured into a solution of 3 ml of 2N hydrochloric acid and 500 ml of water and the aqueous mixture is extracted twice with 100 ml of ethyl acetate each time, and the organic phases are washed twice with 50 ml of water each time, dried over anhydrous sodium sulphate and evaporated to dryness under reduced pressure. The residue is recrystalized from diethyl ether/n-hexane. There is obtained 3-(4-chloro-2-fluoro-5-isopropoxyphenyl)-6-trifluoromethyl-2,4(1H,3H)-pyrimidinedione, m.p. 195°-197° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04812164
출처 데이터셋uspto-grants-1989_03
ORD IDord-216d22aa144349878c456c1d375ec62f
출처 메모uspto-grants-1989_03