戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 227873作成日:2026年10月26日

4'-Bromoacetanilide → N-Acetyl-4-aminobiphenyl

https://huagongshe.com/reaction/227873

反応式

関与物質

役割名称HCID仕込み量
反応物4'-BromoacetanilideHCID 7683—
反応物Phenylboronic AcidHCID 66827—
反応物Potassium FluorideHCID 522689—
触媒palladium(II) acetateHCID 167845—
触媒2-(Di-tert-butylphosphino)biphenylHCID 2734215—
生成物N-Acetyl-4-aminobiphenylHCID 1999886.2%

反応手順

An oven dried resealable Schlenk tube was evacuated and backfilled with argon and charged with palladium acetate (2.2 mg, 0.01 mmol, 1.0 mol %), 2-(di-tert-butylphosphino)biphenyl (6.0 mg, 0.02 mmol, 2.0 mol %), phenylboronic acid (183 mg, 1.5 mmol), potassium fluoride (174 mg, 3.0 mmol), and 4′-bromoacetanilide (214 mg, 1.0 mmol). The tube was evacuated and backfilled with argon, and THF (1 mL) was added through a rubber septum. The tube was sealed with a teflon screwcap, and the reaction mixture was stirred at room temperature until the starting aryl bromide had been completely consumed as judged by GC analysis. The reaction mixture was then diluted with ether (30 mL), filtered through celite, and concentrated. The crude material was purified by flash chromatography on silica gel to afford 182 mg (86%) of the title compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07560582B2
出典データセットuspto-grants-2009_07
ORD IDord-7f9e88ff24594db1b6115af7ca086cf9
出典メモuspto-grants-2009_07