HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanethiol → 2-cyanimino-N-(4-methylbenzyl)-thiazolidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanethiol | HCID 878 | — |
| Reactant | N-(4-methylbenzyl)-cysteamine | HCID 14306202 | — |
| Reactant | Cyanimino-dithiocarbonic acid dimethylester | HCID 87522899 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-cyanimino-N-(4-methylbenzyl)-thiazolidine | HCID 14306206 | 85.5% |
Reaction Steps
3.65 g (23.5 mmoles) of cyanimino-dithiocarbonic acid dimethylester (purity: 94%) and 5.43 g (30 mmoles) of N-(4-methylbenzyl)-cysteamine are boiled in 30 ml of ethanol until the evolution of methyl-mercaptan terminates (about 2 hours). The reaction mixture is evaporated and the crystalline residue is recrystallized from 6 ml of isopropanol. 4.65 g (85.5%) of 2-cyanimino-N-(4-methylbenzyl)-thiazolidine are obtained, melting at 102° to 104° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04616025 |
| Source dataset | uspto-grants-1986_10 |
| ORD ID | ord-5fc881085ec445f88922286ca57db4c8 |
| Source note | uspto-grants-1986_10 |