戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1243317作成日:2026年10月26日

Iodine → 5,6-Dichloro-3-hydroxy-3-(2-methoxyphenyl)-1,3-dihydro-2H-indol-2-one

https://huagongshe.com/reaction/1243317

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MagnesiumHCID 5462224—
反応物5,6-dichloro-1H-indole-2,3-dioneHCID 11009341—
溶媒Diethyl EtherHCID 3283—
溶媒TetrahydrofuranHCID 8028—
生成物5,6-Dichloro-3-hydroxy-3-(2-methoxyphenyl)-1,3-dihydro-2H-indol-2-oneHCID 2192550280.6%

反応手順

7.5 g of 1-bromo-2-methoxybenzene are added dropwise to a suspension of 1.1 g of magnesium in 20 ml of ether containing a few crystals of iodine, the reflux being maintained once it has started. At the end of the addition, the mixture is heated at reflux for 2 hours. A suspension of 4.3 g of 5,6-dichloro-1H-indole-2,3-dione in 20 ml of THF is then added and the resulting mixture is refluxed for 30 minutes. After cooling to RT, the reaction mixture is poured into a water/ice/concentrated HCl mixture and extracted with EtOAc, the organic phase is dried over Na2SO4 and the solvent is evaporated off under vacuum. The residue is triturated in hot iso ether and the precipitate formed is filtered off by suction and washed with ether. 5.2 g of the expected product are obtained, m.p.=245–246° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07119086B2
出典データセットuspto-grants-2006_10
ORD IDord-565d91cc6fda462198d18bd8a8f68e27
出典メモuspto-grants-2006_10