HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenyl Isothiocyanate → N-Butan-2-yl-N-[(4-chlorophenyl)methyl]-N'-phenylthiourea
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenyl Isothiocyanate | HCID 7673 | — |
| Reactant | N-(4-chlorobenzyl)butan-2-amine | HCID 4717029 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | N-Butan-2-yl-N-[(4-chlorophenyl)methyl]-N'-phenylthiourea | HCID 13018270 | 91% |
Reaction Steps
20 g of N-(4-chlorobenzyl)-N-sec.-butylamine were dissolved in 500 ml of ether. To the resulting solution, a solution of 14 g of phenyl isothiocyanate in 50 ml of ether was added dropwise, under cooling and stirring. After the dropwise addition, the temperature of the solution was gradually raised, and the solution was then stirred at room temperature for about 10 hours. The crystals which had been formed were separated by filtration. After recrystallization with a solvent mixture of hexane and ethyl alcohol, 30 g of N-(4-chlorobenzyl)-N-sec.-butyl-N'-phenylthiourea were obtained. Yield: 91%. Melting point: 134°-134.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04036986 |
| Source dataset | uspto-grants-1977_07 |
| ORD ID | ord-8fee94989e1f483d8687b053b84066cc |
| Source note | uspto-grants-1977_07 |