Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 7538Erstellt: 23. Oktober 2026

1-Naphthalenecarbonitrile → Naphthalene-1-carboxamidine hydrochloride

https://huagongshe.com/de/reaction/7538

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-NaphthalenecarbonitrileHCID 6846—
EduktAmmonium ChlorideHCID 25517—
EduktTrimethylaluminumHCID 16682925—
LösungsmittelTolueneHCID 1140—
LösungsmittelDichloromethaneHCID 6344—
LösungsmittelHexaneHCID 8058—
ProduktNaphthalene-1-carboxamidine hydrochlorideHCID 12301252—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

14 g (261 mmol, 2 equiv.) ammonium chloride are suspended in 150 ml of dry toluene under an argon athmosphere, and the mixture is cooled to 0° C. 130 ml (260 mmol, 2 equiv.) of a 2M solution of trimethylaluminium in hexane are added dropwise, and the reaction mixture is stirred at room temperature until no more evolution of gas is observed. After addition of 20 g (130 mmol, 1 equiv.) 1-cyanonaphthalene, the mixture is stirred at 80° C. bath temperature over night. The mixture is cooled and poured into a slurry of silica in methylene chloride. After filtration, the solid is washed with methanol for several times, the solution is evaporated to dryness in vacuo and the residue washed with methanol. The combined filtrates are pooled and stirred in a mixture of methylene chloride containing 10% methanol.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07087605B2
Quelldatensatzuspto-grants-2006_08
ORD IDord-df7e8f4754984965badaea04cfade0f5
Quellennotizuspto-grants-2006_08