HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → N'-[amino(methylsulfanyl)methyl]-N,N-dimethylethanimidamide;hydroiodide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | (E)-1-(dimethylamino)ethylidenethiourea | HCID 10654343 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N'-[amino(methylsulfanyl)methyl]-N,N-dimethylethanimidamide;hydroiodide | HCID 87308795 | 96% |
Reaction Steps
A suspension of (1E)-N′-(aminocarbonothioyl)-N,N-dimethylethanimidamide (47.8 g, 0.33 mole) in methyl iodide (150 mL) and THF (350 mL) was stirred for 18 h at room temperature. The mixture was evaporated under reduced pressure. After addition of 5% MeOH and diethyl ether, the compound precipitated and was collected by filtration affording (1E)-N′-[amino(methylthio)methyl]-N,N-dimethylethanimidamide hydrogen iodide salt (91.0 g, 96% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08044062B2 |
| Source dataset | uspto-grants-2011_10 |
| ORD ID | ord-63b5a68a548b47268a3810896efc568e |
| Source note | uspto-grants-2011_10 |