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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1288518Erstellt: 26. Oktober 2026

Ethanol → [1-Methyl-3-(2,6,6-trimethyl-2-cyclohexenyl)-2(trans)-propenyl]dimethyl(4-chlorobenzyl)ammonium iodide

https://huagongshe.com/reaction/1288518

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthanolHCID 702—
EduktPotassium IodideHCID 4875—
Edukt1-Chloro-4-(chloromethyl)benzeneHCID 7723—
Edukt[1-Methyl-3-(2,6,6-trimethyl-2-cyclohexenyl)-2(trans)-propenyl]dimethylamineHCID 21502510—
LösungsmittelWaterHCID 962—
Produkt[1-Methyl-3-(2,6,6-trimethyl-2-cyclohexenyl)-2(trans)-propenyl]dimethyl(4-chlorobenzyl)ammonium iodideHCID 21502450131,7%

Reaktionsschritte

A mixture of [1-methyl-3-(2,6,6-trimethyl-2-cyclohexenyl)-2-(trans)propenyl]dimethylamine (2.2 g), α,4-dichlorotoluene (0.8 g) and ethanol (30 cc) was refluxed for 1 hour, and thereto were added water (100 cc) and potassium iodide (5.0 g). The reaction mixture was extracted with chloroform, and the chloroform layer was dried over magnesium sulfate. The solvent was distilled off, and the residue was recrystallized from ethanol to give crystals (3.1 g) of [1-methyl-3-(2,6,6-trimethyl-2-cyclohexenyl)-2(trans)-propenyl]dimethyl(4-chlorobenzyl)ammonium iodide.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS03988373
Quelldatensatzuspto-grants-1976_10
ORD IDord-1fafe0e295bc4256a85fda167ac6d9ca
Quellennotizuspto-grants-1976_10