HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanethiol → {3-[(4-Methoxyphenyl)methyl]-1,3-thiazolidin-2-ylidene}cyanamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanethiol | HCID 878 | — |
| Reactant | N-(4-methoxybenzyl)-cysteamine | HCID 14306201 | — |
| Reactant | Cyanimino-dithiocarbonic acid dimethylester | HCID 87522899 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | {3-[(4-Methoxyphenyl)methyl]-1,3-thiazolidin-2-ylidene}cyanamide | HCID 14306204 | 92% |
Reaction Steps
3.65 g (23.5 moles) of cyanimino-dithiocarbonic acid dimethylester (purity: 94%) and 5.91 (30 moles) of N-(4-methoxybenzyl)-cysteamine are boiled in 30 ml of ethanol until the evolution of methyl mercaptan terminates. The reaction mixture is evaporated and the crystalline residue is recrystallized from 15 ml of isopropanol. 5.35 g (92%) of 2-cyanimino-3-(4-methoxybenzyl)-thiazolidine are obtained, melting at 99° to 102° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04616025 |
| Source dataset | uspto-grants-1986_10 |
| ORD ID | ord-da11e47810b3438c9a5b4916232a9061 |
| Source note | uspto-grants-1986_10 |