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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 552302생성일: 2026년 10월 24일

Iodine → 5-Chloro-3-hydroxy-3-(2-methoxyphenyl)indolin-2-one

https://huagongshe.com/ko/reaction/552302

반응식

참여 물질

역할이름HCID투입량
반응물IodineHCID 807—
반응물2-BromoanisoleHCID 11358—
반응물Ammonium ChlorideHCID 25517—
반응물5-chloro-1H-indole-2,3-dioneHCID 87203—
반응물MagnesiumHCID 5462224—
용매WaterHCID 962—
용매Diethyl EtherHCID 3283—
생성물5-Chloro-3-hydroxy-3-(2-methoxyphenyl)indolin-2-oneHCID 21905955—

반응 조건

온도20 °C

반응 단계

40 g (1.65 mol) magnesium shavings were overlaid with 100 ml ether, and after the addition of a small amount of iodine, they were carefully heated until the reaction kicked off. 203 ml (1.65 mol) bromanisole, dissolved in 450 ml ether, were dropped in to the boiling solution so slowly that the reaction continually proceeded at a low boil. Subsequently, with slight cooling to 20° C., 75 g (0.41 mol) 5-chlorisatin in 750 ml water-free tetrahydrofurane were added in by drops. After this, everything was stirred for 30 minutes more at room temperature. The reaction solution was poured into an aqueous NH4Cl solution while being stirred. This aqueous phase was extracted a number of times with ethyl acetate and the combined aqueous phases were washed with water four times, dried and concentrated in a vacuum. The residue obtained was crystallised from isopropanol, wherein 106 g of the intermediate product resulted.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07951807B2
출처 데이터셋uspto-grants-2011_05
ORD IDord-88e0a1f133ca41278c6589fdf10551a2
출처 메모uspto-grants-2011_05