HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → Methyl n,n'-diphenylcarbamimidothioate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Diphenylthiourea | HCID 700999 | — |
| Solvent | Water | HCID 962 | — |
| Product | Methyl n,n'-diphenylcarbamimidothioate | HCID 221767 | — |
Reaction Steps
To a 2 l flask were added 342 g of thiocarbanilide, 240 g of methyl iodide and 350 cc of ethanol and the mixture was refluxed for 2 hours. After cooling the mixture to a room temperature, a small amount of water was added and the mixture was allowed to stand to precipitate the raw product, which was then filtered off and dissolved in 12 l of hot water. After filtration, the filtrate was converted to an alkaline solution by addition of NaOH to precipitate the product. The product was filtered and washed well until the filtrate became neutral. After drying, the product was recrystalized in 1 l of ethanol to give S-methyl-N,N'-diphenylisothiourea.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04387150 |
| Source dataset | uspto-grants-1983_06 |
| ORD ID | ord-1105de70bcdf44d48bde246d90b98bbd |
| Source note | uspto-grants-1983_06 |