HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Thiazolidinone,4-thioxo- → HCID 178508330, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Thiazolidinone,4-thioxo- | HCID 1539595 | — |
| Reactant | HCID 178508669 | HCID 178508669 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 178508330 | HCID 178508330 | — |
Reaction Steps
To a stirred solution of 49.7 parts of 2-oxo-4-thioxothiazolidine in 990 parts of methanol there was added at 40° C. and under an atmosphere of nitrogen 54.3 parts of powdered 1,3-diiminoisoindoline. Initially, a thick slurry resulted. The reaction mixture was stirred at room temperature for two hours during which time the mixture gradually thinned. The mixture was then heated at reflux for approximately two hours and after cooling to 25° C., was filtered. The collected solid was washed with fresh methanol and dried in vacuo at 50° C. to obtain 1-imino-3-(2-oxo-4-thioxo-5-thiazolidinylidene)isoindoline as an orange powder melting at 267°-8° C. (dec.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04028372 |
| Source dataset | uspto-grants-1977_06 |
| ORD ID | ord-22216317c05d493e81fdc0e0761e14fe |
| Source note | uspto-grants-1977_06 |