HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-(Phenylmethyl)-2-thioxo-4-thiazolidinone → 3-Benzyl-5-(3-ethylbenzothiazolylidene)rhodanine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-(Phenylmethyl)-2-thioxo-4-thiazolidinone | HCID 97673 | — |
| Reactant | 2-Ethylmercapto-3-ethylbenzothiazolium | HCID 170396 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | 3-Benzyl-5-(3-ethylbenzothiazolylidene)rhodanine | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04356247 |
| Source dataset | uspto-grants-1982_10 |
| ORD ID | ord-0520e0008641406897ad4aef1d831a68 |
| Source note | uspto-grants-1982_10 |