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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 336864생성일: 2026년 10월 24일

Hydrochloric Acid → Ethyl 6-chloro-4-hydroxy-3-quinolinecarboxylate

https://huagongshe.com/ko/reaction/336864

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물4-ChloroanilineHCID 7812—
반응물Sodium HydroxideHCID 14798—
반응물3-Ethoxy-2-ethoxycarbonylprop-2-enoateHCID 85829211—
용매WaterHCID 962—
용매Ethyl AcetateHCID 8857—
생성물Ethyl 6-chloro-4-hydroxy-3-quinolinecarboxylateHCID 71811371%

반응 단계

A mixture of 4-chloroaniline (156.7 mmol) and ethyl ethoxymethylenemalonate (156.7 mmol) was stirred at room temperature until homogeneous. The homogeneous solution was heated in an oil bath at 165° C. for 6 hours. The reaction mixture was cooled to room temperature and 1 N HCl (3 mL) was added. The reaction mixture was stirred and heated to 115° C. for 3 hours. The mixture was cooled to room temperature and then treated with 20 mL of water. The resulting suspension treated with 10 N NaOH solutions to reach the pH about 8. It was partitioned between ethyl acetate and water. The organic layer was separated and the aqueous layer was extracted with ethyl acetate. The combined organic extracts were washed with brine, dried over MgSO4, filtered and concentrated. The crude product was purified by flash column chromatography using a 9:1 v/v hexane: ethyl acetate as solvent to afford title compound (28 g, 71% yield) as a yellow solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08889706B2
출처 데이터셋uspto-grants-2014_11
ORD IDord-e6dd59b80fae4a7cafa0105fa0fca600
출처 메모uspto-grants-2014_11