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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2294796Generated: October 25, 2026

2-Chlorobenzoyl chloride → 3-(2-Chlorobenzoyl)-1-phenyl-imidazolidin-2,4-dione

https://huagongshe.com/reaction/2294796

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chlorobenzoyl chlorideHCID 69110—
Reactant1-Phenylimidazolidine-2,4-dioneHCID 570576—
SolventPyridineHCID 1049—
Product3-(2-Chlorobenzoyl)-1-phenyl-imidazolidin-2,4-dioneHCID 2147218713%

Reaction Steps

In a similar manner to Example 8, 560 mg (3.18 mmol) of 1-phenyl-imidazolidin-2,4-dione were reacted with 560 mg (3.22 mmol) of 2-chlorobenzoyl chloride. After completion of the reaction, pyridine was distilled off under reduced pressure, and the resultant residue was subjected to extraction with ethyl acetate. The organic layer was washed with dilute hydrochloric acid and with saturated saline. The thus-washed organic layer was dried over anhydrous magnesium sulfate, and the solvent was then distilled off. The resultant residue was purified by column chromatography on silica gel (developing solvent: methylene chloride) and subjected to crystallization from n-hexane/ethyl acetate to obtain 130 mg (yield: 12.9%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05691335
Source datasetuspto-grants-1997_11
ORD IDord-c03abd8f4def4823a4020e1ca7a9b90b
Source noteuspto-grants-1997_11