Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 638678Erstellt: 26. Oktober 2026

Ammonium → Ethylene

https://huagongshe.com/reaction/638678

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAmmoniumHCID 223—
EduktImidazolium cationHCID 444234—
EduktPyridiniumHCID 4989215—
EduktPhosphoniumHCID 5460504—
Edukt1H-imidazol-3-ium chlorideHCID 66617091—
LösungsmittelBenzeneHCID 241—
LösungsmittelTolueneHCID 1140—
LösungsmittelAluminum(III) ChlorideHCID 6451240—
LösungsmittelHCID 178462722HCID 178462722—
ProduktEthyleneHCID 6325—
ProduktEthylbenzeneHCID 7500—

Reaktionsschritte

An acidic reactant also known is an acidic ionic liquid, which is a salt having a melting point of less than 100° C., can be used in Friedel-Crafts reactions as well. The systems employed to date are those formed by adding a molar excess of a Lewis acid to the halide salt of an imidazolium, pyridinium, ammonium, or phosphonium ion. One example is a mixture of Imidazolium chloride salt with a molar excess of AlCl3. These acidic chloroaluminate molten substances are used to catalyze organic reactions in place of solid AlCl3, so that the disadvantage of the low solubility of AlCl3 in most organic solvents Is minimized. Examples in the literature include the reaction of benzene and toluene with various alkyl chlorides in a mixture of 1-ethyl-3-methylimidazolium chloride ([EMIM]Cl) and AlCl3 (4 parts [EMIM]Cl/6 parts AlCl3); and the alkylation of benzene with ethylene to form ethylbenzene using a liquid catalyst phase that is a mixture of an imidazolium chloride salt having a molar excess of AlCl3 or a molar excess of GaCl3.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07691180B2
Quelldatensatzuspto-grants-2010_04
ORD IDord-0a7bf25d698049fe8b43d8a8e76b065e
Quellennotizuspto-grants-2010_04