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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2169212Generated: November 1, 2026

1-Naphthaleneacetonitrile → HCID 13980433, compound

https://huagongshe.com/reaction/2169212

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-NaphthaleneacetonitrileHCID 8596—
ReactantAmmonium ChlorideHCID 25517—
ReactantTrimethylaluminumHCID 16682925—
SolventTolueneHCID 1140—
ProductHCID 13980433HCID 1398043391%

Reaction Steps

To a stirred suspension of NH4Cl (1.6 g, 30 mmol) in anhydrous toluene (50 mL) was added trimethyl aluminium (2M in toluene, 15 mL, 30 mmol) at 0° C. The mixture was then warmed to room temperature and stirred for 2 h. A solution of 2-(naphthalen-1-yl)acetonitrile (1.67 g, 10 mmol) in toluene (10 mL) was added to the above reaction mixture and the reaction mixture was stirred at 80° C. for 18 h. After completion of the reaction, the reaction mixture was quenched with a suspension of silica gel in chloroform. The mixture was stirred at room temperature for 0.5 h before being filtered through a sintered funnel. The silica gel was washed with methanol. The combined filtrate was concentrated under reduced pressure to give the crude product as an off-white solid (2 g, 91%), which was used directly without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09045486B2
Source datasetuspto-grants-2015_06
ORD IDord-51a1a775da9c4588a6853e16b34ffd23
Source noteuspto-grants-2015_06