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 2 hours. The reaction mixture was cooled to room temperature, diluted with water (10-15 ml.) 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 | US04031127 |
| Source dataset | uspto-grants-1977_06 |
| ORD ID | ord-96f4a1d08c0b4bdabafb7d5b2fee3fb8 |
| Source note | uspto-grants-1977_06 |