HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzene, 1-isothiocyanato-4-nitro- → N-Cyano-N'-(4-nitrophenyl)thiourea
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzene, 1-isothiocyanato-4-nitro- | HCID 75044 | — |
| Reactant | Cyanamidnatrium | HCID 57375518 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | N-Cyano-N'-(4-nitrophenyl)thiourea | HCID 14569042 | 61.2% |
Reaction Steps
The suspension of monosodium cyanamide (6.4 g, 100 mmol) in absolute ethanol (170 mL) was slowly treated with (4-nitrophenyl)isothiocyanate (12.5 mL, 104.5 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 (13.6 g), m.p. >250° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05140031 |
| Source dataset | uspto-grants-1992_08 |
| ORD ID | ord-dbe4af745a2a47ab910cb1248befce9f |
| Source note | uspto-grants-1992_08 |