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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2306170Generated: November 2, 2026

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

https://huagongshe.com/reaction/2306170

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 numberUS06441017B1
Source datasetuspto-grants-2002_08
ORD IDord-ad6b1ea289df4d9aa8e99df86dd7cfe3
Source noteuspto-grants-2002_08