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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1610835Generated: November 1, 2026

Benzoyl chloride → HCID 22258292, compound

https://huagongshe.com/reaction/1610835

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
Reactant5-Ethyl-2,4-dimethyl-1H-imidazoleHCID 15724086—
SolventAcetonitrileHCID 6342—
ProductHCID 22258292HCID 22258292—

Reaction Steps

The compound is prepared as described in example X (step 4 and 5) with 1.00 g (8.05 mmol) 4-Ethyl-2,5-dimethyl-1H-imidazole (example XIII, step 1), 3.74 g (26.57 mmol) of benzoyl chloride and 2.85 g (28.18 mmol) of TEA in 20 ml acetonitrile. After reaction the solvent is evaporated under vacuum. The residue is extracted with toluene/water and the water phase is filtrated over a silica-layer. The solvent is evaporated under vacuum. The crude intermediate is directly transformed into 2-(4-Ethyl-5-methyl-1H-imidazol-2-yl)-1-phenylethanone hydrochloride. After the reaction the solvent is evaporated under vacuum. The residue is extracted with ethyl acetate/water. The water phase is concentrated.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06984646B2
Source datasetuspto-grants-2006_01
ORD IDord-8e24d90ed3234f5f9f0c5c6110af8157
Source noteuspto-grants-2006_01