HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → HCID 19979632, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | HCID 19979627 | HCID 19979627 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 19979632 | HCID 19979632 | — |
Reaction Steps
5 g of N-[2,6-dimethyl-4-(4-trifluoromethylthiazol-2-yloxy)phenyl]-N'-tert-butylthiourea are heated in 30 ml of ethanol and 2.1 g of iodomethane for 5 hours to 50° C. The alcohol is subsequently removed by evaporation and the residue is taken up in methylene chloride. The methylene chloride solution is washed twice with dilute sodium carbonate solution and dried over sodium sulfate. The solvent is removed by evaporation and the residue is recrystallised from hexane, affording the title compound of formula ##STR35## with a melting point of 88°-90° C. (compound 4.01).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04888348 |
| Source dataset | uspto-grants-1989_12 |
| ORD ID | ord-9d03ba51731b47ae9c89a06fb08fe47d |
| Source note | uspto-grants-1989_12 |