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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 443214Generated: October 30, 2026

Triethylamine → 4-[(5-Formylimidazol-1-yl)methyl]benzonitrile

https://huagongshe.com/reaction/443214

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthyl AcetateHCID 8857—
Reactant1-(4-Cyanobenzyl)-5-hydroxymethyl-1H-imidazoleHCID 10198247—
SolventDimethyl SulfoxideHCID 679—
Product4-[(5-Formylimidazol-1-yl)methyl]benzonitrileHCID 10632289—

Reaction Steps

To a solution of the alcohol from Step D (21.5 g, 101 mol) in DMSO (500 ml) at room temperature was added triethylamine 56 ml, 402 mmol), then SO3 -pyridine complex (40.5 g, 254 mmol). After 45 min, the reaction was poured into EtOAc, washed with water and brine, dried (Na2SO4), and concentrated in vacuo to provide the aldehyde as a white powder which was sufficiently pure without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05891889
Source datasetuspto-grants-1999_04
ORD IDord-b5eea04c267b42069af37b45fdb8d6df
Source noteuspto-grants-1999_04