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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 5544생성일: 2026년 10월 23일

4,7-Dichloroquinoline → 7-Chloro-4-(4-fluorophenoxy)quinoline

https://huagongshe.com/ko/reaction/5544

반응식

참여 물질

역할이름HCID투입량
반응물4,7-DichloroquinolineHCID 6866—
반응물4-FluorophenolHCID 9732—
반응물4-PyrrolidinopyridineHCID 75567—
용매O-XyleneHCID 7237—
생성물7-Chloro-4-(4-fluorophenoxy)quinolineHCID 164171649.9%

반응 단계

To a 50 mL flask equipped with a condenser, drying tube and thermometer, was added 1.98 g (0.01 moles) of 4,7-dichloroquinoline, 1.57 g (0.0014 moles) of 4-fluorophenol, 0.22 g (0.0015 moles) of 4-pyrrolidinopyridine and 20 mL of xylene. The reaction mixture was heated to reflux and reaction progress was monitored by TLC. After 18 hr, the mixture was cooled and washed with 50 mL of 5 N NaOH. The caustic layer was extracted with 3×20 mL of diethyl ether. The xylene and the ether layers were combined and dried over Na2SO4. Removal of the solvent provided 2.49 g (91 percent yield) of product, mp=88°-91° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05245036
출처 데이터셋uspto-grants-1993_09
ORD IDord-083e912021ea4636b30489d9253b9684
출처 메모uspto-grants-1993_09