Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1682118Generated: October 31, 2026

Benzaldehyde → HCID 15224426, compound

https://huagongshe.com/reaction/1682118

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
ReactantDeaminoimiquimodHCID 11424651—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductHCID 15224426HCID 15224426—

Reaction Conditions

Temperature-78 °C

Reaction Steps

1-(2-Methylpropyl)-1H-imidazo[4,5-c]quinoline (4 g; 0.017 mole) was dissolved in 50 mL of tetrahydrofuran then cooled to -78° C. A 7.75 mL portion of n-butyl lithium (2.5M in hexanes) was added dropwise to the cooled solution. At 15 minutes post addition, benzaldehyde (2.7 mL; 0.027 mole) was added and the reaction mixture was allowed to warm slightly. The reaction was quenched with water then diluted with ethyl ether. The ether was separated, dried with magnesium sulfate then concentrated under vacuum. The resulting residue was purified by silica gel chromatography using 5% methanol in methylene chloride as the eluent to give an oily yellow solid. This material was recrystallized from methylene chloride/hexane to provide 1-(2-Methylpropyl)-α-phenyl-1H-imidazo[4,5-c]quinoline-2-methanol as a white crystalline solid, m.p. 160°-166° C. Analysis: Calc'd: C, 76.1; H, 6.4; N, 12.7; Found: C, 75.9; H, 6.3; N, 12.7.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05175296
Source datasetuspto-grants-1992_12
ORD IDord-e6e36dc739664249ab55288b40f8d6f5
Source noteuspto-grants-1992_12