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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 21815Erstellt: 23. Oktober 2026

Allyl chloride → alpha-Allyl-alpha-isopropyl-2-methylbenzyl cyanide

https://huagongshe.com/de/reaction/21815

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAllyl chlorideHCID 7850—
EduktSodium HydroxideHCID 14798—
Edukt3-Methyl-2-(2-methylphenyl)butanenitrileHCID 14245130—
KatalysatorTetrabutylammonium hydrogen sulfateHCID 94433—
LösungsmittelWaterHCID 962—
Produktalpha-Allyl-alpha-isopropyl-2-methylbenzyl cyanideHCID 1993353193%

Reaktionsbedingungen

Temperatur40 °C

Reaktionsschritte

To a solution of 362 g of sodium hydroxide in 362 ml of demineralized water 216.6 g of α-isopropyl-2-methylbenzyl cyanide and 6.4 g of tetrabutylammonium hydrogen sulfate were added, and the mixture was heated to 40° C. with intensive stirring. During 3hours 287 g of allylchloride was added. During, the addition and for further two hours the temperature of the reaction mixture was maintained at 40° C. and thereafter at 60° C. for additional three hours. After cooling to room temperature, the reaction mixture was diluted with 550 ml of water and the product was extracted into toluene. After washing with water until neutral pH and drying with anhydrous magnesium sulfate, the solvent was evaporated and the residue was distilled under diminished pressure to obtain 249 g (93%) of the desired compound, b.p. 122°-124 ° C./333 Pa.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05424456
Quelldatensatzuspto-grants-1995_06
ORD IDord-4885e1af76354a0da3de3354ae290034
Quellennotizuspto-grants-1995_06