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HRID 219754作成日:2026年10月25日

Iodine → 3-(2-Ethoxyphenyl)-3-hydroxy-5-iodoindol-2-one

https://huagongshe.com/reaction/219754

反応式

関与物質

役割名称HCID仕込み量
反応物IodineHCID 807—
反応物Ammonium ChlorideHCID 25517—
反応物2-BromophenetoleHCID 68500—
反応物5-IodoisatinHCID 88695—
反応物MagnesiumHCID 5462224—
溶媒Diethyl EtherHCID 3283—
溶媒TetrahydrofuranHCID 8028—
生成物3-(2-Ethoxyphenyl)-3-hydroxy-5-iodoindol-2-oneHCID 57466442—

反応条件

温度20 °C

反応手順

4 g (164 mMol) of magnesium turnings and 5% of the total amount of 2-bromo-1-ethoxybenzene were put into 20 ml of ether and, after addition of a little iodine, were heated until the reaction started. 33.1 g (165 mMol) of 2-bromo-1-ethoxybenzene dissolved in 100 ml of ether were slowly added dropwise to the boiling solution in such a way that the reaction continued with gentle boiling. Then, while cooling slightly to 20° C., 15 g (54.9 mMol) of 5-iodoisatin in 400 ml of anhydrous tetrahydrofuran were added dropwise. The mixture was then stirred at room temperature for 2 h. The reaction solution was poured into an aqueous NH4Cl solution with stirring. This aqueous phase was extracted several times with ethyl acetate, and the combined aqueous phase was washed four times with water, dried and concentrated in vacuo, resulting in the product as a crystalline precipitate. 19.2 g of the product were obtained.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08202870B2
出典データセットuspto-grants-2012_06
ORD IDord-f588b2f796754e5b9d1ed63240c9f62f
出典メモuspto-grants-2012_06