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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1016544Generated: October 25, 2026

Dichloromethane → 2-(4-Chlorophenyl)imino-5-methyl-5-phenyl-3-phenylaminothiazolidin-4-one

https://huagongshe.com/reaction/1016544

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
Reactant4-ChloroanilineHCID 7812—
ReactantTriethyloxonium tetrafluoroborateHCID 2723982—
Reactant5-Methyl-5-phenyl-3-phenylamino-2-thioxothiazolidin-4-oneHCID 12056392—
SolventWaterHCID 962—
SolventChloroformHCID 6212—
Product2-(4-Chlorophenyl)imino-5-methyl-5-phenyl-3-phenylaminothiazolidin-4-oneHCID 1205639957.8%

Reaction Steps

5-Methyl-5-phenyl-3-phenylamino-2-thioxothiazolidin-4-one (0.28 g) was mixed with a 1M methylene chloride solution of triethyloxonium tetrafluoroborate (1 ml) at room temperature. The reaction mixture was stirred for 24 hrs at room temperature then p-chloroaniline (0.25 g) in chloroform (10 ml) was added to the mixture at 0° C. The mixture was stirred at room temperature for 1 hr and then water was added. The separated oil was extracted with chloroform. The chloroform layer was dried over anhydrous magnesium sulfate and the solvent was evaporated under reduced pressure. The residue was purified by column chromatography (chloroform-n-hexane, 1/1) to yield 2-(4-chlorophenyl)imino-5-methyl-5-phenyl-3-phenylaminothiazolidin-4-one (0.21 g) having a melting point of 53-54° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06476055B1
Source datasetuspto-grants-2002_11
ORD IDord-105d2b56416140af9ee08bc5a39791ea
Source noteuspto-grants-2002_11