Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1241490Generated: October 25, 2026

1-Naphthalenecarbonitrile → Naphthalene-1-carboxamidine hydrochloride

https://huagongshe.com/reaction/1241490

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 atmosphere, 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-cyano-naphthalene, 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 numberUS07115602B2
Source datasetuspto-grants-2006_10
ORD IDord-5cce14ab66ff41abacd992fb80e7f618
Source noteuspto-grants-2006_10