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HRID 500133作成日:2026年10月26日

N,N,N',N'-Tetramethylethylenediamine → 4-Acetyl-2-fluorobenzonitrile

https://huagongshe.com/reaction/500133

反応式

関与物質

役割名称HCID仕込み量
反応物N,N,N',N'-TetramethylethylenediamineHCID 8037—
反応物1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 636044—
反応物1-(4-Bromo-3-fluorophenyl)ethan-1-oneHCID 22831914—
触媒Zinc cyanide (Zn(CN)2)HCID 11186—
触媒Bis(dibenzylideneacetone)palladiumHCID 9811564—
溶媒DimethylformamideHCID 6228—
生成物4-Acetyl-2-fluorobenzonitrileHCID 22481653—

反応条件

温度160 °C

反応手順

N,N,N′,N′-Tetramethylethylenediamine (0.667 mL, 4.42 mmol), zinc cyanide (1.46 g, 12.4 mmol), tris(dibenzylideneacetone)dipalladium(0) (54.05 mg, 0.059 mmol) and (9,9-dimethyl-9H-xanthene-4,5-diyl)bis(diphenylphosphine) (124.3 mg, 0.215 mmol) was added successively to a solution of 1-(4-bromo-3-fluorophenyl)ethanone (4.34 g, 20.0 mmol) in N,N-dimethylformamide (15 mL) in a microwave tube. The tube was sealed and degassed three times, and heated to 160° C. under microwave irradiation with a 240 s hold time, and 300 Watt maximum power input. After cooling, the reaction mixture was filtered through a pad of Celite with a thin layer of silica gel in the middle using dichloromethane as the eluant. The combined filtrates were concentrated under reduced pressure. The residue was purified by chromatography on silica gel with ethyl acetate in hexanes (0-40%) to give the desired product. (3.20 g, 98.1%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07767675B2
出典データセットuspto-grants-2010_08
ORD IDord-77ff4e5b5c7244ae8e31d1c30552ca0c
出典メモuspto-grants-2010_08