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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1935408Generated: October 31, 2026

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

https://huagongshe.com/reaction/1935408

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 the alcohol from Step D (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 which was sufficiently pure for use in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06387903B1
Source datasetuspto-grants-2002_05
ORD IDord-18ecabb8979f47b091743774b2478060
Source noteuspto-grants-2002_05