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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 394239Erstellt: 25. Oktober 2026

Sodium Cyanide → [2-(4-Isopropyl-phenyl)-thiazol-4-yl]-acetonitrile

https://huagongshe.com/reaction/394239

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium CyanideHCID 8929—
Edukt1,3-DichloroacetoneHCID 10793—
Edukt4-(Propan-2-yl)benzene-1-carbothioamideHCID 2078831—
Edukt4-Chloromethyl-2-(4-isopropyl-phenyl)-thiazoleHCID 2095697—
LösungsmittelDimethyl SulfoxideHCID 679—
LösungsmittelWaterHCID 962—
Produkt[2-(4-Isopropyl-phenyl)-thiazol-4-yl]-acetonitrileHCID 2264762396%

Reaktionsbedingungen

Temperatur40 °C

Reaktionsschritte

14.5 g (57.6 mmol) of 4-chloromethyl-2-(4-isopropyl-phenyl)-thiazole (prepared from 4-isopropyl-thiobenzamide and 1,3-dichloroacetone in analogy to the procedure described in example 4 a]) and 4.08 g (83.4 mmol) of sodium cyanide in 50 ml of dimethyl sulfoxide were stirred at 40° C. for 2 hours. Then, the reaction mixture was poured into a mixture of ice and water and was subsequently extracted with 3 portions of 75 ml of tert-butyl methyl ether. The combined organic phases were washed with water, then with brine and dried with anhydrous sodium sulfate. After evaporation of the solvent, 13.4 g (96% of theory) of [2-(4-isopropyl-phenyl)-thiazol-4-yl]-acetonitrile were obtained as brown solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06809110B2
Quelldatensatzuspto-grants-2004_10
ORD IDord-6febcf5681e248c295525a601d837e59
Quellennotizuspto-grants-2004_10