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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 506488생성일: 2026년 10월 25일

Ammonium Chloride → Ethyl 4-chloro-3-hydroxy-5-phenyl-2-(4-fluoro-2-trifluoromethylbenzoylamino)pent-4-enoate

https://huagongshe.com/reaction/506488

반응식

참여 물질

역할이름HCID투입량
반응물Ammonium ChlorideHCID 25517—
반응물Lithium diisopropylamideHCID 2724682—
반응물2-ChlorocinnamaldehydeHCID 3014042—
반응물Ethyl (4-fluoro-2-trifluoromethylbenzoylamino)acetateHCID 59432157—
용매TetrahydrofuranHCID 8028—
생성물Ethyl 4-chloro-3-hydroxy-5-phenyl-2-(4-fluoro-2-trifluoromethylbenzoylamino)pent-4-enoateHCID 72297221—

반응 조건

온도-75 °C

반응 단계

At −75° C., 5.0 g (0.0170 mol) of ethyl (4-fluoro-2-trifluoromethylbenzoylamino)acetate dissolved in THF were added dropwise to 25.0 ml (0.050 mol) of a 2M solution of lithium diisopropylamide in THF. After 1 h at −75° C., 3.50 g (0.021 mol) of 2-chlorocinnamaldehyde dissolved in THF were added dropwise, and the mixture was stirred at −75° C. for 1 h. Saturated NH4Cl solution was added dropwise and the mixture was warmed to RT and extracted with CH2Cl2. The combined organic phases were washed and dried, and the solvent was removed. The residue was purified chromatographically (SiO2, cyclohexane/ethyl acetate). This gave 7.5 g (96% of theory) of the title compound as a colorless solid (diastereomer mixture) which was reacted further without further purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07786046B2
출처 데이터셋uspto-grants-2010_08
ORD IDord-c28b6902540445b687345a44a4ead64e
출처 메모uspto-grants-2010_08