Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2422526Generated: November 3, 2026

1,4-Dioxane → 7-Formyl-4-phenylquinoline-2-carbonitrile

https://huagongshe.com/reaction/2422526

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-DioxaneHCID 31275—
Reactant7-(Dibromomethyl)-4-phenylquinoline-2-carbonitrileHCID 66790248—
CatalystSilver NitrateHCID 24470—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
Product7-Formyl-4-phenylquinoline-2-carbonitrileHCID 57437845—

Reaction Steps

To a solution of 7-(dibromomethyl)-4-phenylquinoline-2-carbonitrile (2.02 g, 4.81 mmol) in 1,4-dioxane (75 mL) was added a solution of silver nitrate (3.27 g, 19.24 mmol) in 30 mL of water, and the reaction mixture stirred 1 h at reflux. After cooling to rt, the mixture was diluted with EtOAc and filtered. The solid was washed with EtOAc and the organic phases combined. The filtrate was washed twice with water and the combined aqueous layers were back-extracted twice with EtOAc. The combined organic extracts were washed with brine, dried over MgSO4, filtered and concentrated. The crude residue obtained was purified by column chromatography (eluting with acetone-CH2Cl2-toluene, 10:40:50) to yield the title compound. 1H NMR (400 MHz, acetone-d6): δ 10.39 (s, 1H), 8.80 (s, 1H), 8.21 (s, 2H), 8.07 (s, 1H), 7.66 (m, 5H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07960409B2
Source datasetuspto-grants-2011_06
ORD IDord-76026457846243138282583150962968
Source noteuspto-grants-2011_06