돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 11632생성일: 2026년 10월 24일

Potassium Iodide → 2-(4-Chloro-2-nitro-phenoxy)-1-[4-(4-fluoro-benzyl)-(2R,5S)-2,5-dimethyl-piperazin-1-yl]-ethanone

https://huagongshe.com/ko/reaction/11632

반응식

참여 물질

역할이름HCID투입량
반응물Potassium IodideHCID 4875—
반응물4-Chloro-2-nitrophenolHCID 6980—
반응물Potassium CarbonateHCID 11430—
반응물2-Chloro-1-[4-(4-fluoro-benzyl)-(2R,5S)-2,5-dimethyl-piperazin-1-yl]-ethanoneHCID 11358461—
용매WaterHCID 962—
용매Methyl Ethyl KetoneHCID 6569—
생성물2-(4-Chloro-2-nitro-phenoxy)-1-[4-(4-fluoro-benzyl)-(2R,5S)-2,5-dimethyl-piperazin-1-yl]-ethanoneHCID 4443152592.5%

반응 단계

To a solution of 2-chloro-1-[4-(4-fluoro-benzyl)-(2R,5S)-2,5-dimethyl-piperazin-1-yl]-ethanone (1.0 g, 3.35 mmol) in butanone (35 mL) was added 2-nitro-4-chlorophenol (0.64 g, 3.69 mmol), potassium carbonate (0.93 g, 6.7mmol) and potassium iodide (0.56 g, 3.35 mmol). The reaction mixture was heated at reflux overnight. The reaction mixture was then cooled, diluted with water and extracted with ethyl acetate. The organic layer was dried over magnesium sulfate, filtered and concentrated to give an orange oil. Chromatography on silica gel gave the title compound (1.35 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07098212B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-25061445411d408e8604d629580259c9
출처 메모uspto-grants-2006_08