HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → 1-{4-[2-(4-Chlorobenzoyl)hydrazino]phenyl}-3-phenylthiourea
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Phenyl Isothiocyanate | HCID 7673 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | 1-(Chlorobenzoyl)-2-(4-aminophenyl)hydrazine hydrochloride | HCID 21427838 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1-{4-[2-(4-Chlorobenzoyl)hydrazino]phenyl}-3-phenylthiourea | HCID 21427840 | — |
Reaction Steps
1-(Chlorobenzoyl)-2-(4-aminophenyl)hydrazine hydrochloride (2.0 g, 0.0067 mole) was mixed with ethanol (125 ml) and water (25 ml). Phenyl isothiocyanate (1.1 g, 0.01 mole) was added to the mixture along with sodium acetate (0.82 g, 0.01 mole) in water (10 ml). The reaction mixture was stirred and refluxed for 5 minutes, then was stirred at room temperature for one and one half hours. The mixture was chilled in ice and then filtered. The product was washed with ethanol and dried to give an off-white solid. Yield 1.9 g (71%), m.p. 197.5°-199° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04030925 |
| Source dataset | uspto-grants-1977_06 |
| ORD ID | ord-cd7af99808f64daaa269d933a11a90ed |
| Source note | uspto-grants-1977_06 |