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HRID 1270728作成日:2026年10月27日

N-bromobutanimide → 4-Bromo-3,5-difluoroaniline

https://huagongshe.com/reaction/1270728

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3,5-DifluoroanilineHCID 96595—
溶媒Diethyl EtherHCID 3283—
溶媒DimethylformamideHCID 6228—
生成物4-Bromo-3,5-difluoroanilineHCID 2736260—

反応手順

3,5-Difluoroaniline (10.0 g, 77.5 mmol) is dissolved in DMF (100 mL). NBS (13.9 g, 78.0 mmol) is added portionwise at room temperature. After stirring overnight at room temperature, the reaction mixture is diluted with Et2O and washed with brine. The separated organic phase is dried (Na2SO4) and concentrated to give an oil which is purified by column chromatography (methylene chloride/hexanes) to give 4-bromo-3,5-difluoroaniline.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07202364B2
出典データセットuspto-grants-2007_04
ORD IDord-e552a0d6f13146c99cc37f51be6c777b
出典メモuspto-grants-2007_04