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HRID 500133Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/500133

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktN,N,N',N'-TetramethylethylenediamineHCID 8037—
Edukt1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 636044—
Edukt1-(4-Bromo-3-fluorophenyl)ethan-1-oneHCID 22831914—
KatalysatorZinc cyanide (Zn(CN)2)HCID 11186—
KatalysatorBis(dibenzylideneacetone)palladiumHCID 9811564—
LösungsmittelDimethylformamideHCID 6228—
Produkt4-Acetyl-2-fluorobenzonitrileHCID 22481653—

Reaktionsbedingungen

Temperatur160 °C

Reaktionsschritte

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%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07767675B2
Quelldatensatzuspto-grants-2010_08
ORD IDord-77ff4e5b5c7244ae8e31d1c30552ca0c
Quellennotizuspto-grants-2010_08