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HRID 601768作成日:2026年10月26日

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

https://huagongshe.com/reaction/601768

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Diethyl EtherHCID 3283—
溶媒TetrahydrofuranHCID 8028—
生成物5-Chloro-3-hydroxy-3-(2-methoxyphenyl)indolin-2-oneHCID 2190595589.2%

反応条件

温度21 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07902379B2
出典データセットuspto-grants-2011_03
ORD IDord-d27efc37f2e44cfb8528f7a662d313bd
出典メモuspto-grants-2011_03