HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Isothiocyanate → 1-Benzyl-3-phenyl-2-thiourea
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Isothiocyanate | HCID 2346 | — |
| Reactant | Aniline | HCID 6115 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 1-Benzyl-3-phenyl-2-thiourea | HCID 668300 | — |
Reaction Steps
To a stirred solution of 74.6 g (0.5 mol) of benzylisothiocyanate in 500 mL toluene was added dropwise 46.6 g (0.5 mol) of aniline. The solution was refluxed 18 hours. After cooling, the reaction mixture was concentrated under reduced pressure. The residue was recrystallized from an appropriate solvent to yield N-phenyl-N'-benzylthiourea. Isothiocyanates which are not commercially available may be prepared from aliphatic or aryl primary amines by the following methods: Kurita and Iwakura, Org. Synth. 59, 195; Jochims, Chem. Ber. 101, 1746 (1968); or Castro, Pena, Santos, and Vega, J. Org. Chem. 49, 863 (1984).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04971983 |
| Source dataset | uspto-grants-1990_11 |
| ORD ID | ord-6c43c8ac9d91418ab2318252c6e42559 |
| Source note | uspto-grants-1990_11 |