HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenyl Isothiocyanate → N-(3-Methyl-1,3-thiazolidin-2-ylidene)-N'-phenylthiourea
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenyl Isothiocyanate | HCID 7673 | — |
| Reactant | 3-Methyl-1,3-thiazolidin-2-imine hydroiodide | HCID 2770507 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | N-(3-Methyl-1,3-thiazolidin-2-ylidene)-N'-phenylthiourea | HCID 54546998 | — |
Reaction Steps
Sodium methoxide (2.16 g) was added to a mixture of 2-imino-3-methylthiazolidine hydroiodide (10.0 g) in ethanol (50 ml) and brought to reflux, with stirring. Phenylisothiocyanate (5.4 g) in ethanol (20 ml) was added to the mixture over 5 minutes and the resultant mixture heated under reflux, with stirring, for one hour then cooled in ice. Filteration gave analytically pure product, mpt 169°-170°, which may be recrystallised from isopropanol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04250173 |
| Source dataset | uspto-grants-1981_02 |
| ORD ID | ord-bbf1b3724acf419abc9d1f16a86dfde4 |
| Source note | uspto-grants-1981_02 |