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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 374263Erstellt: 24. Oktober 2026

Hydrochloric Acid → 2-Chloro-3-(2-methyl-3-trifluoromethylphenyl)-propionitrile

https://huagongshe.com/de/reaction/374263

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktAcrylonitrileHCID 7855—
EduktTrifluoromethyl toluidineHCID 2735932—
EduktSodium NitriteHCID 23668193—
KatalysatorCopper oxideHCID 14829—
LösungsmittelWaterHCID 962—
LösungsmittelDichloromethaneHCID 6344—
Produkt2-Chloro-3-(2-methyl-3-trifluoromethylphenyl)-propionitrileHCID 1980964290,1%

Reaktionsbedingungen

Temperatur20 °C

Reaktionsschritte

20 mol of concentrated hydrochloric acid is added at 0°-5° C. to a suspension of 16.7 g of 2-methyl-3-trifluoromethylaniline (0.095 mol) in 50 ml mixture is then briefly warmed to 60°-80° C. until a clear solution has formed. The solution is cooled very rapidly to 0°-5° C. with vigorous stirring, 22.4 ml (0.286 mol) of acrylonitrile are added dropwise to the fine suspension at 0°-5° C. and a solution of 6.75 g of sodium nitrite in 10 ml of water is then rapidly added, and the mixture is kept at 5° C. for a further 5 minutes and stirred at 20° C for 1 hour. After cooling, 0.8 g of copper(II) oxide powder is added to the reaction mixture at 0°-10° C. in portions, a vigorous evolution of nitrogen gas occurring. After completion of the evolution of gas, the mixture is stirred for a further 2 hours at 0°-10° C., then for 15 hours at room temperature, dichloromethane is added, and the mixture is washed with water, dried over sodium sulphate and concentrated in vacuo. 21.2 g (90% of theory) of 2-chloro-3-(2-methyl-3-trifluoromethylphenyl)-propionitrile are obtained as a brown oil. M/e 247 (M+), 228, 212, 173 (100%)

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05166395
Quelldatensatzuspto-grants-1992_11
ORD IDord-4c9fd72cd36149eb9b0bb8a9aec43639
Quellennotizuspto-grants-1992_11