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HRID 31353作成日:2026年10月24日

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

https://huagongshe.com/ja/reaction/31353

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 2192550274%

反応手順

5.57 g of 1-bromo-2-methoxybenzene are added dropwise to a suspension of 0.72 g of magnesium in 15 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 refluxed for 2 hours. A suspension of 2.7 g of 5,6-dichloro-1H-indole-2,3-dione in 30 ml of THF is then added and the 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 slurried in hot iso ether and the precipitate formed is spin-filtered off and washed with ether. 3 g of the expected product are obtained.

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-8a70d1b019c341bfa8531040820b3ea8
出典メモuspto-grants-2008_09