HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,1-Bis(methylthio)-2-nitroethylene → 3-Benzyl-2-nitromethylene-thiazolidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,1-Bis(methylthio)-2-nitroethylene | HCID 83623 | — |
| Reactant | Ethanethiol, 2-benzylamino- | HCID 136802 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 3-Benzyl-2-nitromethylene-thiazolidine | HCID 3024396 | 95.8% |
Reaction Steps
3.34 g (20 moles) of N-benzyl-cysteamine and 3.3 g of 1,1-bis-methylthio-2-nitro-ethylene are refluxed in 50 ml of ethanol for one hour. The gas evolution terminates after boiling for 20 minutes. The mixture is cooled and the precipitated product is isolated by filtration. 4.52 g of 3-benzyl-2-nitromethylene-thiazolidine are obtained, melting at 136° to 138° C. Crystallization of the product from 140 ml of ethanol yields 4.08 g of a purified product, melting at 139° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04616025 |
| Source dataset | uspto-grants-1986_10 |
| ORD ID | ord-7cdd1e28a5fc45739c3ae95110efa5e3 |
| Source note | uspto-grants-1986_10 |