Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 223757Generated: October 30, 2026

3-(Phenylmethyl)-2-thioxo-4-thiazolidinone → 3-Benzyl-5-(3-ethylbenzothiazolylidene)rhodanine

https://huagongshe.com/reaction/223757

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(Phenylmethyl)-2-thioxo-4-thiazolidinoneHCID 97673—
Reactant2-Ethylmercapto-3-ethylbenzothiazoliumHCID 170396—
SolventTriethylamineHCID 8471—
Product3-Benzyl-5-(3-ethylbenzothiazolylidene)rhodanineHCID 86738612—

Reaction Steps

To 30 ml of an ethanol solution of 13.0 g of the intermediate product obtained in Preparative Example 2, viz., 2-ethylmercapto-3-ethylbenzothiazolium p-toluenesulfoante, was added 4.5 g of 3-benzylrhodanine, while stirring the mixture at room temperature (about 20° C.), 6.1 g of triethylamine was added dropwise to the mixture over a 3 minute period, and thereafter, the resultant mixture was refluxed for 10 minutes. After cooling the reaction mixture, precipitate formed was recovered by filtration and recrystallized from a mixture of chloroform and ethanol to provide 4.6 g of 3-benzyl-5-(3-ethylbenzothiazolylidene)rhodanine (melting point 209° to 211° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04356247
Source datasetuspto-grants-1982_10
ORD IDord-0520e0008641406897ad4aef1d831a68
Source noteuspto-grants-1982_10