HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → HCID 178503941, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | N-(((2,6-Dichlorophenyl)amino)thioxomethyl)benzamide | HCID 702451 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 178503941 | HCID 178503941 | 85% |
Reaction Steps
19.5 g (0.06 M) of N-(2,6-dichlorophenyl)-N'-benzoyl thiourea, 5.5 g (0.04 M) of ground potassium carbonate, 5.1 ml (0.08 M) of methyliodide and 200 ml of acetone are boiled in a reflux for 4 hours under energetic shaking. The acetone is distilled off. 200 ml of water are added to the residue and it is then filtered. The sediment on the filter is washed to a neutral pH. After drying 20.2 g (99% of the theoretical yield) of N-(2,6-dichlorophenyl)-N'-benzoyl-S-methylisothiourea are obtained with melting point 127-129° C. This product being recrystallized from ethyl alcohol gives the corresponding isothiourea with a melting point of 128°-130° C. and 85% yield of the theoretical one.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04290971 |
| Source dataset | uspto-grants-1981_09 |
| ORD ID | ord-ef15b820fb874719afa9d02dcf3f0d1c |
| Source note | uspto-grants-1981_09 |