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HRID 983004作成日:2026年10月26日

Water → 4-Phenylindolin-2-one

https://huagongshe.com/reaction/983004

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物4-Phenyl-1H-indoleHCID 15806298—
反応物PyridiniumtribromideHCID 21124087—
触媒ZincHCID 23994—
溶媒Acetic AcidHCID 176—
溶媒EthanolHCID 702—
溶媒tert-ButanolHCID 6386—
生成物4-Phenylindolin-2-oneHCID 1304860167%

反応手順

To the suspension of 4-phenyl-1H-indole (1.1 g, 5.7 mmol) in 2-methyl-2-propanol (33 mL), ethanol (22 mL) and acetic acid (11 mL) was added pyridinium tribromide (90% purity from Aldrich, 6.1 g, 17.1 mmol) portionwise over 10 minutes. The mixture was stirred at room temperature for 2 hours, and then to the mixture was added acetic acid (50 mL). After stirring at room temperature for one hour, water (0.5 mL) and zinc (3.7 g, 57 mmol) were added to the reaction mixture and stirring was continued for another hour. The unreacted zinc dust was filtered off and washed with methanol. The filtrate was concentrated and the syrupy residue was suspended in water (100 mL) for overnight. The solid product was filtered, washed repeatedly with water to remove the zinc salt and pyridine salt. After high vacuum dry, 800 mg (67%) of 4-phenyl-1,3-dihydro-indol-2-one as a light yellow solid was obtained.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06861418B2
出典データセットuspto-grants-2005_03
ORD IDord-019143f702134c938a561e745cea973f
出典メモuspto-grants-2005_03