HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Chloro-2-isothiocyanatobenzene → N-(2-chlorophenyl)-N'-cyanothiourea
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Chloro-2-isothiocyanatobenzene | HCID 123171 | — |
| Reactant | Cyanamidnatrium | HCID 57375518 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | N-(2-chlorophenyl)-N'-cyanothiourea | HCID 11769784 | 96.4% |
Reaction Steps
The suspension of monosodium cyanamide (1.9 g, 29.4 mmol) in absolute ethanol (50 mL) was slowly treated with 2-chlorophenylisothiocyanate (5.0 g, 29.4 mmol). The reaction was allowed to stir at room temperature for 1 hour and then heated at 75° C. for 4 hours. The reaction was cooled to room temperature and the colorless solid was filtered and washed with ethanol to give the title A compound (6.0 g), m.p. 253°-255° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05140031 |
| Source dataset | uspto-grants-1992_08 |
| ORD ID | ord-4ed00b5e462c488db6a4cc5e226ede5f |
| Source note | uspto-grants-1992_08 |