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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 7538Generated: October 26, 2026

1-Naphthalenecarbonitrile → Naphthalene-1-carboxamidine hydrochloride

https://huagongshe.com/reaction/7538

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-NaphthalenecarbonitrileHCID 6846—
ReactantAmmonium ChlorideHCID 25517—
ReactantTrimethylaluminumHCID 16682925—
SolventTolueneHCID 1140—
SolventDichloromethaneHCID 6344—
SolventHexaneHCID 8058—
ProductNaphthalene-1-carboxamidine hydrochlorideHCID 12301252—

Reaction Conditions

Temperature0 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07087605B2
Source datasetuspto-grants-2006_08
ORD IDord-df7e8f4754984965badaea04cfade0f5
Source noteuspto-grants-2006_08