HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzoyl chloride → Thiourea, [3-(dimethylamino)-2-methylphenyl]-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzoyl chloride | HCID 7412 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Potassium thiocyanate | HCID 516872 | — |
| Reactant | 1,3-Benzenediamine,N,N,2-trimethyl-(9CI) | HCID 11137341 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | Thiourea, [3-(dimethylamino)-2-methylphenyl]- | HCID 10856728 | 91.3% |
Reaction Steps
57 g of 3-dimethylamino-2-methyl-aniline, 1.15 liters of acetone, 36.6 g of KSCN and 43.8 ml of benzoylchloride are refluxed together for 3 hours. After cooling to ambient temperature the reaction mixture is poured onto 2.4 kg of crushed ice. The precipitate obtained is heated to 60° C. for 2 hours together with 85 g of KOH, 85 ml of water and 255 ml of ethanol. After the addition of 850 ml of water the ethanol is distilled off under reduced pressure. After the resulting precipitate has been worked up, 72 g of N-(3-dimethylamino-2-methylphenyl)-thiourea are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06858594B2 |
| Source dataset | uspto-grants-2005_02 |
| ORD ID | ord-4af9c31168e94a3c9a00a55a1e5628d3 |
| Source note | uspto-grants-2005_02 |