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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2073883Generated: October 30, 2026

4-(4-(2-Quinolinylmethyloxy)styryl)benzonitrile → 4-(4-(2-Quinolinylmethyloxy)phenethyl)benzonitrile

https://huagongshe.com/reaction/2073883

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(4-(2-Quinolinylmethyloxy)styryl)benzonitrileHCID 54295323—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product4-(4-(2-Quinolinylmethyloxy)phenethyl)benzonitrileHCID 14995004—

Reaction Steps

A mixture of 0.75 g (2.07 mmol) of (4-(4-(2-quinolinylmethyloxy)styryl)benzonitrile and 0.08 g of 10% Pd on carbon in 75 ml of ethanol is shaken for 1.5 hours under 30 PSI of hydrogen. The mixture is filtered through a bed of celite and the filtrate concentrated in vacuo. Trituration with ether gives a precipitate which is filtered off and recrystallized from methylene chloride-ether to give 4-(4-(2-quinolinylmethyloxy)phenethyl)benzonitrile. (M.P. 156° C.-158° C.)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04920133
Source datasetuspto-grants-1990_04
ORD IDord-a8b69b11fe27439892842099d862044e
Source noteuspto-grants-1990_04