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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2187873Generated: October 31, 2026

Triethylamine → 1-(4-Cyano-3-fluorobenzyl)-5-imidazolecarboxaldehyde

https://huagongshe.com/reaction/2187873

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthyl AcetateHCID 8857—
Reactant1-(4-Cyano-3-fluorobenzyl)-5-(hydroxymethyl)imidazoleHCID 18536062—
SolventDimethyl SulfoxideHCID 679—
Product1-(4-Cyano-3-fluorobenzyl)-5-imidazolecarboxaldehydeHCID 11424708—

Reaction Steps

To a solution of 1-(4-cyano-3-fluorobenzyl)-5-(hydroxymethyl)imidazole, as described above in Step F, (2.31 g, 10.0 mmol) in 20 mL of DMSO at 0° C. was added triethylamine (5.6 mL, 40 mmol), then SO3-pyridine complex (3.89 g, 25 mmol). After 30 minutes, the reaction was poured into EtOAc, washed with water and brine, dried (Na2SO4), filtered, and concentrated in vacuo to provide the aldehyde as a pale yellow powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06410534B1
Source datasetuspto-grants-2002_06
ORD IDord-3036bbab612b44ceb83c6b4d963b67e4
Source noteuspto-grants-2002_06