HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → HCID 178484955, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Hydrogen iodide | HCID 24841 | — |
| Reactant | HCID 20466711 | HCID 20466711 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 178484955 | HCID 178484955 | — |
Reaction Steps
N-Methyl-N'-[4-(2-thiazolyl)butyl]thiourea was converted into its hydriodide salt with 66% hydriodic acid. This salt was dissolved in methanol, methyl iodide added and the solution heated under reflux for 2 hours. Concentration and crystallisation of the resultant oil gave N,S-dimethyl-N'-[4-(2-thiazolyl)butyl]isothiourea dihydriodide. Reaction of this isothiourea with hydroxylamine by the procedure of Example 1(ii) gave the title product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04160030 |
| Source dataset | uspto-grants-1979_07 |
| ORD ID | ord-bb67a372cf7142cf945a29b1bb77d02a |
| Source note | uspto-grants-1979_07 |