HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Chlorophenyl isothiocyanate → N-(4-Chlorophenyl)-N'-cyanothiourea
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Chlorophenyl isothiocyanate | HCID 16480 | — |
| Reactant | Cyanamidnatrium | HCID 57375518 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | N-(4-Chlorophenyl)-N'-cyanothiourea | HCID 11805994 | 86.8% |
Reaction Steps
The suspension of monosodium cyanamide (1.9 g, 29.4 mmol) in absolute ethanol (5 mL) was slowly treated with 4-chlorophenylisothiocyanate (5.0 g, 29.4 mmol). The reaction was allowed to stir at room temperature for one hour and then heated at 75° C. for four hours. The reaction was cooled to room temperature and the colorless solid was filtered and washed with ethanol to give the title compound (5.4 g), mp>250° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05612323 |
| Source dataset | uspto-grants-1997_03 |
| ORD ID | ord-ec5b337ad6ff45189ab98bde3205f48e |
| Source note | uspto-grants-1997_03 |