Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1422346Generated: November 1, 2026

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

https://huagongshe.com/reaction/1422346

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 mmol) 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 minutes, the reaction was poured into 2.5 L of EtOAc, washed with water (4×1 L) and brine, dried, (Na2SO4), and concentrated in vacuo to provide the aldehyde as a white powder which was sufficiently pure for use in the next step without further purificaton.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06080870
Source datasetuspto-grants-2000_06
ORD IDord-5115de033b564d35a5d1cf5202240504
Source noteuspto-grants-2000_06