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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 423105Erstellt: 25. Oktober 2026

4-Chlorobenzonitrile → (Z)-1-(4-chlorophenyl)-2-(thiazol-2-yl)ethenamine

https://huagongshe.com/reaction/423105

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-ChlorobenzonitrileHCID 12163—
Eduktn-Butyl lithiumHCID 61028—
Edukt2-MethylthiazoleHCID 77129—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt(Z)-1-(4-chlorophenyl)-2-(thiazol-2-yl)ethenamineHCID 5775030631%

Reaktionsbedingungen

Temperatur-70 °C

Reaktionsschritte

A 2.5M solution of N-butyllithium (8.00 mL, 20.00 mmol) in hexanes, was added dropwise to 2-methylthiazole (1.983 g, 20 mmol) dissolved in THF (35.00 mL) over a period of 5 minutes under argon at −70° C. The resulting pale yellow slurry was stirred at −70° C. for 2.5 hour. 4-chlorobenzonitrile (2.75 g, 20.00 mmol) in THF (35.00 mL) was added dropwise to the suspension, which was stirred at −70° C. for 90 minutes after the end of the addition. The reaction mixture was allowed to warm to room temperature under stirring and darkened. The crude was concentrated to dryness and diluted with ethyl acetate then washed with water, dried over magnesium sulphate and concentrated. The crude product was purified by flash chromatography on silica gel eluting with 10 to 100% ethyl acetate in dichloromethane. The solvent was evaporated to dryness to afford (Z)-1-(4-chlorophenyl)-2-(thiazol-2-yl)ethenamine (1.466 g, 31.0%) as a pale yellow solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08101623B2
Quelldatensatzuspto-grants-2012_01
ORD IDord-39b6bfe9ef8a414ea5978e6c0eb883e2
Quellennotizuspto-grants-2012_01