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HRID 49121作成日:2026年10月24日

Ethanol → 5-Phenyloxindole

https://huagongshe.com/ja/reaction/49121

反応式

関与物質

役割名称HCID仕込み量
反応物EthanolHCID 702—
反応物Sodium CarbonateHCID 10340—
反応物Phenylboronic AcidHCID 66827—
反応物5-Bromo-2-oxindoleHCID 611193—
触媒Tetrakis(triphenylphosphine)palladiumHCID 11979704—
溶媒TolueneHCID 1140—
溶媒Ethyl AcetateHCID 8857—
生成物5-PhenyloxindoleHCID 1330197877.3%

反応条件

温度100 °C

反応手順

5-Bromo-2-oxindole (5 g, 23.5 mmol) was dissolved in 110 mL of toluene and 110 mL of ethanol with stirring and a little heating. Tetrakis(triphenylphosphine)-palladium(0) (1.9 g, 1.6 mmol) was added followed by a 2M aq. solution of sodium carbonate (40 mL, 80 mmol). To this mixture benzene boronic acid (3.7 g, 30.6 mmol) was added and the mixture was heated in a 100° C. oil bath. After 12 h, the reaction was diluted with ethyl acetate (500 mL), washed with saturated aq. sodium bicarbonate (200 mL), water (200 mL), 1N HCl (200 mL) and brine (200 mL). The organic layer was dried with magnesium sulfate and concentrated to afford a brown solid. Trituration with dichloromethane and filtering afforded 3.8 g (77%) of a tan solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06706709B2
出典データセットuspto-grants-2004_03
ORD IDord-53c59fa6a8fe410f8728af630b8a9eb8
出典メモuspto-grants-2004_03