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HRID 552302作成日:2026年10月25日

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

https://huagongshe.com/reaction/552302

反応式

関与物質

役割名称HCID仕込み量
反応物IodineHCID 807—
反応物2-BromoanisoleHCID 11358—
反応物Ammonium ChlorideHCID 25517—
反応物5-chloro-1H-indole-2,3-dioneHCID 87203—
反応物MagnesiumHCID 5462224—
溶媒WaterHCID 962—
溶媒Diethyl EtherHCID 3283—
生成物5-Chloro-3-hydroxy-3-(2-methoxyphenyl)indolin-2-oneHCID 21905955—

反応条件

温度20 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07951807B2
出典データセットuspto-grants-2011_05
ORD IDord-88e0a1f133ca41278c6589fdf10551a2
出典メモuspto-grants-2011_05