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HRID 219762作成日:2026年10月27日

Water → 3-Hydroxy-4,6-dichloro-1,3-dihydro-3-(4-trifluoromethylphenyl)indol-2-one

https://huagongshe.com/reaction/219762

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Benzene, 1-bromo-4-(trifluoromethyl)-HCID 67872—
反応物4,6-DichloroisatinHCID 251908—
反応物MagnesiumHCID 5462224—
溶媒Diethyl EtherHCID 3283—
溶媒TetrahydrofuranHCID 8028—
生成物3-Hydroxy-4,6-dichloro-1,3-dihydro-3-(4-trifluoromethylphenyl)indol-2-oneHCID 66602670—

反応手順

1.8 g of Grignard magnesium are placed in 19 ml of anhydrous ethyl ether in a round-bottomed flask equipped with a mechanical stirrer, and under a stream of nitrogen. A mixture of 8.9 ml of 4-bromotrifluoromethylbenzene in 46 ml of anhydrous ethyl ether is then added. The mixture is stirred for one hour, followed by addition of a solution of 5.7 g of 4,6-dichloro-1H-indole-2,3-dione in 100 ml of anhydrous THF. The mixture is stirred at room temperature for 4 hours 30 minutes. Water is added and the resulting mixture is extracted with ethyl acetate. The organic phase is separated out and dried over Na2SO4, filtered and evaporated under vacuum. The residue is taken up in ethyl acetate and washed with 1N sodium hydroxide solution. The organic phase is dried over Na2SO4, filtered and evaporated under vacuum. The solid is taken up in ethyl ether and filtered off. 4.7 g of expected product are obtained.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08202871B2
出典データセットuspto-grants-2012_06
ORD IDord-15e2988c599d4d829b0be32d5a2db277
出典メモuspto-grants-2012_06