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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2227448Generated: October 30, 2026

Ethyl Acetate → HCID 18473741, compound

https://huagongshe.com/reaction/2227448

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantHCID 18473749HCID 18473749—
SolventThionyl ChlorideHCID 24386—
ProductHCID 18473741HCID 18473741—

Reaction Steps

N-{2-[2-(4-Cyanophenyl)-ethyl]-1-methyl-benzimidazol-5-yl}-(4-carboxy-benzenesulphonamide) (2.0 g, 4.3 mmol) is refluxed in 10 mL thionyl chloride for 1.5 h. The mixture is diluted with 50 mL ethyl acetate, the crystalline hydrochloride of the acid chloride is filtered off and washed with ethyl acetate/diethylether. The solid is suspended in 40 mL ethanol and slowly brought to reflux temperature. Half the ethanol is distilled off, the remainder is cooled and combined with ice water and made alkaline with aqueous potassium carbonate solution with stirring. It is diluted with water, the solid is filtered off and washed with water.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06413990B1
Source datasetuspto-grants-2002_07
ORD IDord-d4fe802941ac4bb3ad171437715dc1e7
Source noteuspto-grants-2002_07