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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1741498Generated: November 1, 2026

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

https://huagongshe.com/reaction/1741498

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) in 500 mL of DMSO at room temperature was added triethylamine (56 mL), then SO3 -pyridine complex (40.5 g). After 45 minutes, the reaction was poured into 2.5 L of EtOAc, washed with water (4×1 L) and brine, dried (Na2SO4), filtered, and concentrated in vacuo to provide the titled aldehyde as a white powder which was sufficiently pure for use in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05972984
Source datasetuspto-grants-1999_10
ORD IDord-7d4e7863c9ad476bbb2ea1a08ad9716b
Source noteuspto-grants-1999_10