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HRID 7889作成日:2026年10月25日

N-bromobutanimide → 4-Bromo-2-butyl-6-fluoro-5-hydroxy-1-indanone

https://huagongshe.com/reaction/7889

反応式

関与物質

役割名称HCID仕込み量
反応物N-bromobutanimideHCID 67184—
反応物2-Butyl-6-fluoro-5-hydroxy-1-indanoneHCID 21990885—
溶媒DimethylformamideHCID 6228—
生成物4-Bromo-2-butyl-6-fluoro-5-hydroxy-1-indanoneHCID 2199085290.9%

反応手順

N-Bromosuccinimide (1.41 g, 7.93 mmol) was added to a solution of 2-butyl-6-fluoro-5-hydroxy-1-indanone (1.76 g, 7.93 mmol) in anhydrous N,N-dimethylformamide (15 mL). The resulting solution was stirred at room temperature for two hours. The solvent was evaporated under vacuum and the residue was partitioned between EtOAc (100 mL) and water (100 ml). The organic phase was washed with water (4×100 mL) and brine (50 mL), dried over MgSO4, filtered, and evaporated under vacuum to provide crude 4-bromo-2-butyl-6-fluoro-5-hydroxy-1-indanone (2.17 g) as an oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07087599B2
出典データセットuspto-grants-2006_08
ORD IDord-003b390b794440cdb243ce9841e7b453
出典メモuspto-grants-2006_08