HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → Hydrogen iodide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | HCID 73840649 | HCID 73840649 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Hydrogen iodide | HCID 24841 | — |
| Product | HCID 54448851 | HCID 54448851 | — |
Reaction Steps
5 g of 1-benzylideneamino-imidazolidine-2-thion are suspended in 40 ml of methanol and treated with 1.7 ml of methyliodide. The mixture obtained is refluxed for ca. one hour and the solvent is evaporated off. 1-Benzylideneamino-2-methylthio-4,5-dihydro-1H-imidazole in the form of a hydroiodide is obtained in solid form, to which 120 ml of water and 70 ml of an anion exchange resin in chloride form (Amberlite IRA-400 (Cl)R) are added. The mixture is stirred for ca. 2 hours at room temperature, filtrated and lyophilized. 1-Benzylideneamino-2-methylthio-4,5-dihydro-1H-imidazole in the form of a hydrochloride is obtained in the form of a lyophilisate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06440957B1 |
| Source dataset | uspto-grants-2002_08 |
| ORD ID | ord-b515248b040f428f877b420dff66edaf |
| Source note | uspto-grants-2002_08 |