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HRID 31342作成日:2026年10月24日

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

https://huagongshe.com/ja/reaction/31342

反応式

関与物質

役割名称HCID仕込み量
反応物Diethyl EtherHCID 3283—
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TetrahydrofuranHCID 8028—
生成物5-Chloro-3-hydroxy-3-(2-methoxyphenyl)indolin-2-oneHCID 21905955—
生成物HCID 178489560HCID 178489560—

反応手順

This compound is prepared according to the procedure disclosed in WO 95/18105. A solution of 2-methoxyphenylmagnesium bromide is prepared from 16 g of magnesium in 35 ml of ether and from a solution of 124 g of 1-bromo-2-methoxybenzene in 175 ml of ether. This solution is added dropwise under an argon atmosphere to a mixture, cooled beforehand in an ice bath, of 30 g of 5-chloro-1H-indole-2,3-dione in 250 ml of THF and then the mixture is left stirring while allowing the temperature to rise to RT. After stirring for 1 hour at RT, the reaction mixture is slowly poured into saturated NH4Cl solution and the THF is evaporated off under vacuum. The precipitate formed is spin-filtered off and is washed with iso ether. 42 g of the expected product are obtained, which product is used without further purification in the following stage.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07425566B2
出典データセットuspto-grants-2008_09
ORD IDord-63ed12e504da457c9655396a881f37c0
出典メモuspto-grants-2008_09