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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 231653생성일: 2026년 10월 25일

Ethanol → 2-([1,1'-Biphenyl]-4-yl)-6-fluoro-3-hydroxyquinoline-4-carboxylic acid

https://huagongshe.com/reaction/231653

반응식

참여 물질

역할이름HCID투입량
반응물EthanolHCID 702—
반응물Sodium HydroxideHCID 14798—
반응물5-FluoroisatinHCID 236566—
반응물Acetic acid 2-biphenyl-2-yl-2-oxo-ethyl esterHCID 20034058—
용매WaterHCID 962—
생성물2-([1,1'-Biphenyl]-4-yl)-6-fluoro-3-hydroxyquinoline-4-carboxylic acidHCID 14498146—

반응 단계

A suspension of 6.6 g of 5-fluoro-2,3-indolinedione in 48 ml of water was treated with a sufficient amount of a solution of 6.62 g of sodium hydroxide in 22 ml of water to provide solution. A warm solution of 10.17 g of acetoxyacetylbiphenyl in 80 ml of ethanol was added, followed by the balance of the alkali solution. The mixture was refluxed for 3 hours. During the last 1/2 hour 10 ml of ethanol was distilled off. A 103 ml portion of water was added, the mixture was stirred, cooled and filtered through diatomaceous earth. The filtrate was treated with 13.6 ml of concentrated hydrochloric acid and 4.39 ml of glacial acetic acid and stirred for 30 minutes. The resulting precipitate was collected, washed with water and ether and air dried. The resulting solid was stirred and heated in 400 ml of ethanol. The solid was collected, washed with water and dried giving 11.2 g of the desired product, mp 25220 -254° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04847381
출처 데이터셋uspto-grants-1989_07
ORD IDord-6428a7d6028a46bf9d567d517a046ff6
출처 메모uspto-grants-1989_07