HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Isothiocyanate → 3-Benzyl-1-{4-[2-(4-chlorobenzoyl)hydrazino]phenyl}thiourea
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Isothiocyanate | HCID 2346 | — |
| Reactant | Potassium Acetate | HCID 517044 | — |
| Reactant | 1-(4-Chlorobenzoyl)-2-(4-aminophenyl)hydrazine hydrochloride | HCID 21427826 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-Benzyl-1-{4-[2-(4-chlorobenzoyl)hydrazino]phenyl}thiourea | HCID 21427828 | — |
Reaction Steps
1-(4-Chlorobenzoyl)-2-(4-aminophenyl)hydrazine hydrochloride (1.5 g, 0.005 mole) was dissolved in hot ethanol (30 ml) under a nitrogen atmosphere. Benzyl isothiocyanate (0.82 g, 0.0055 mole) and potassium acetate (0.6 g, 0.006 mole) were added and the mixture was refluxed under nitrogen for two hours. The reaction mixture was cooled to room temperature, diluted with water (10-15ml.) and chilled in ice. The product was filtered off, washed with ethanol and dried. Recrystallization of the product from acetonitrile gave an off-white solid. Yield 1.25 g (62%), m.p. 197°-199° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04030925 |
| Source dataset | uspto-grants-1977_06 |
| ORD ID | ord-475e63bf55054847bb92a0909d706045 |
| Source note | uspto-grants-1977_06 |