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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1742824Generated: October 31, 2026

Benzoyl chloride → 5-(4-Benzoylaminophenyl)thiazolidine-2,4-dione

https://huagongshe.com/reaction/1742824

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
Reactant1,4-DioxaneHCID 31275—
Reactant5-(4-Aminophenyl)thiazolidine-2,4-dioneHCID 12850972—
SolventTriethylamineHCID 8471—
Product5-(4-Benzoylaminophenyl)thiazolidine-2,4-dioneHCID 1900605993.3%

Reaction Steps

Into 20 ml of dioxane were dissolved 0.5 g of 5-(4-aminophenyl) thiazolidine-2,4-dione, and, after added 0.34 g of benzoyl chloride and further added dropwise 0.24 g of triethylamine, the mixture was refluxed for 1 hour. After cooling by standing, the reaction mixture was poured into 150 ml of ice water and the crystals deposited were collected by filtration, washed with water and dried. These were recrystallized from chloroform to obtain 0.70 g of title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05342850
Source datasetuspto-grants-1994_08
ORD IDord-9beb242176cd4c92aac25d7e1e4edc8e
Source noteuspto-grants-1994_08