HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → 2-Methylsulfanyl-1,4,5,6-tetrahydropyrimidin-3-ium iodide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Tetrahydropyrimidine-2-thione | HCID 2723785 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2-Methylsulfanyl-1,4,5,6-tetrahydropyrimidin-3-ium iodide | HCID 67400810 | — |
Reaction Steps
The reaction mixture comprising one equivalent of 3,4,5,6-tetrahydro(1H)pyrimidine-2-thione and 1.2 equivalents of iodomethane in methanol (10 ml/g of thio-urea) is heated under reflux for 5 hours. After cooling down, the methanol is evaporated off under reduced pressure in order to quantitatively produce the product. The precipitate can then be washed in acetone or petroleum ether.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08012985B2 |
| Source dataset | uspto-grants-2011_09 |
| ORD ID | ord-b3ca276ca2674d24863e666cc2a28267 |
| Source note | uspto-grants-2011_09 |