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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2088667Erstellt: 27. Oktober 2026

Acetonitrile → 3-Amino-3-(2,4-dichlorophenyl)acrylonitrile

https://huagongshe.com/reaction/2088667

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetonitrileHCID 6342—
EduktDiisopropylamineHCID 7912—
Eduktn-Butyl lithiumHCID 61028—
Edukt2,4-DichlorobenzonitrileHCID 81050—
LösungsmittelWaterHCID 962—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt3-Amino-3-(2,4-dichlorophenyl)acrylonitrileHCID 66911322—

Reaktionsschritte

Under argon, 90 g (889.46 mmol) of diisopropylamine were initially charged in 1660 ml of THF at −70° C. in a three-necked flask with mechanical stirrer. 124.66 ml of N-butyllithium solution (2.5 M in hexane, 758.66 mmol) were added dropwise at such a rate that the temperature did not exceed −60° C. The mixture was stirred for 10 min, and a solution of 32.22 g (784.82 mmol) of acetonitrile in 340 ml of THF was then slowly added dropwise and the suspension was stirred for 30 min. A solution of 90 g (523.21 mmol) of 2,4-dichlorobenzonitrile in 340 ml of THF was then added dropwise, and the mixture was stirred at −70° C. for 20 min. The mixture was allowed to slowly warm to RT and stirred at RT for a further 16 h. 600 ml of water were added, most of the THF was distilled off and water and dichloromethane were added. The organic phase was washed with saturated aqueous sodium chloride solution. Removal of the solvent gave crystals which were purified by trituration with diethyl ether. This gave 76.5 g (69% of theory) of the product as a solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08436003B2
Quelldatensatzuspto-grants-2013_05
ORD IDord-cebb1e0ed83a4ba4b6d18e0e701c5e20
Quellennotizuspto-grants-2013_05