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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 601768생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/601768

반응식

참여 물질

역할이름HCID투입량
반응물IodineHCID 807—
반응물2-BromoanisoleHCID 11358—
반응물Ammonium ChlorideHCID 25517—
반응물5-chloro-1H-indole-2,3-dioneHCID 87203—
반응물MagnesiumHCID 5462224—
용매Diethyl EtherHCID 3283—
용매TetrahydrofuranHCID 8028—
생성물5-Chloro-3-hydroxy-3-(2-methoxyphenyl)indolin-2-oneHCID 2190595589.2%

반응 조건

온도21 °C

반응 단계

Magnesium turnings (40 g, 1.65 mol) are introduced into diethyl ether (100 ml) and, while stirring, a solution of 2-bromoanisole (206 ml, 1.65 mol) in diethyl ether (450 ml) is added dropwise. The reaction can be initiated, if necessary, by adding iodine crystals. During the addition, the reaction mixture should boil gently. After the addition, the mixture was stirred at room temperature for 1 hour. A slurry of 5-chloroisatin (75 g, 0.41 mol) in THF (750 ml) was added to the Grignard solution while cooling slightly (temperature 18-24° C.), and the mixture was stirred at room temperature for 30 min. The reaction mixture was stirred into ammonium chloride solution and extracted several times with ethyl acetate. The combined organic phase was washed four times with water, dried over magnesium sulfate and concentrated under reduced pressure. The remaining residue was stirred with 2-propanol. The resulting precipitate was filtered off, washed with 2-propanol and diethyl ether and dried. 106 g of the desired intermediate were obtained.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07902379B2
출처 데이터셋uspto-grants-2011_03
ORD IDord-d27efc37f2e44cfb8528f7a662d313bd
출처 메모uspto-grants-2011_03