HuagongsheHuagongshe Chemistry Print Report · For research reference only
Butyl bromide → HCID 178454975, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Butyl bromide | HCID 8002 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 12952276 | HCID 12952276 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 178454975 | HCID 178454975 | — |
Reaction Steps
5.2 g (0.02 M) of N-(2,6-dichlorophenyl)-N'-acetyl-thiourea, 2.1 ml (0.015 M) of ground potassium carbonate, 3.2 ml (0.03 M) of n-butylbromide and 50 ml of acetone are boiled in a reflux under energetic shaking for 4 hours. The acetone is distilled off. The residue in the flask is washed with water and filtered. 5.8 g (90.6% of the theoretical yield) of N-(2,6-dichlorophenyl)-N'-acetyl-S-n-butylisothiourea with a melting point of 84°-89° are obtained. After recrystallization from ethanol the product has a melting point of 97°-100°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04290971 |
| Source dataset | uspto-grants-1981_09 |
| ORD ID | ord-2a2aa526e9f94d58a0af317e037d9e3c |
| Source note | uspto-grants-1981_09 |