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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1016542Generated: October 26, 2026

Dichloromethane → 2-Hydroxyimino-5-methyl-5-phenyl-3-phenylaminothiazolidine-4-one

https://huagongshe.com/reaction/1016542

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantHydroxyamine hydrochlorideHCID 443297—
ReactantTriethyloxonium tetrafluoroborateHCID 2723982—
Reactant5-Methyl-5-phenyl-3-phenylamino-2-thioxothiazolidin-4-oneHCID 12056392—
SolventMethanolHCID 887—
SolventTriethylamineHCID 8471—
Product2-Hydroxyimino-5-methyl-5-phenyl-3-phenylaminothiazolidine-4-oneHCID 8658849770.2%

Reaction Steps

5-Methyl-5-phenyl-3-phenylamino-2-thioxothiazolidin-4-one (0.3 g) was added to a 1M methylene chloride solution of triethyloxonium tetrafluoroborate (1 ml) at room temperature with stirring. After stirring the mixture for 24 hrs hydroxylamine hydrochloride (0.1 g) and triethylamine (0.3 g) in methanol (10 ml) were added at 0° C. The reaction mixture was again stirred for 2 hrs at room temperature followed by evaporation of the solvents under reduced pressure. The residue was added to ice water and then extracted with ethyl acetate. The ethyl acetate solution was dried over anhydrous ethyl acetate and the solvent was then evaporated under reduced pressure. The residue was purified by column chromatography (ethyl acetate-n-hexane, 1/2) to yield 2-hydroxyimino-5-methyl-5-phenyl-3-phenylaminothiazolidine-4-one (0.21 g) having a melting point of 62-63° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06476055B1
Source datasetuspto-grants-2002_11
ORD IDord-d34e7776f8b34d13ab760266d23eccd7
Source noteuspto-grants-2002_11