HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 413730Generated: October 30, 2026
Phenyl Isothiocyanate → HCID 18521791, compound
https://huagongshe.com/reaction/413730
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phenyl Isothiocyanate | HCID 7673 | — |
| Reactant | Cyanamide | HCID 9864 | — |
| Reactant | 2-Bromo-1-(3-nitrophenyl)ethan-1-one | HCID 75213 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 18521791 | HCID 18521791 | 77.8% |
Reaction Steps
Following the procedure of Gewald et al., J. Prakt. Chem., vol. 35 (1967), pp. 97-104, sodium (188 mg, 8.20 mmol) was carefully dissolved in methanol (9 mL) at 0° C. and allowed to warm to ambient temperature. The resultant solution was added portionwise to a mixture of cyanamide (345 mg, 8.20 mmol) and phenyl isothiocyanate (0.98 mL, 8.2 mmol), whereupon heat evolved. 2-Bromo-3′-nitroacetophenone (2.00 g, 8.2 mmol) was added, and the resultant mixture stirred overnight at ambient temperature. The mixture was diluted with water (150 mL). A yellow-brown solid was filtered off, rinsed with water and a small amount of ether, dried under vacuum, and recrystallized from ethanol to give 2.17 g (52% yield) of the title compound in the form of dark brown crystals, melting point (mp) 186-187° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06569878B1 |
|---|
| Source dataset | uspto-grants-2003_05 |
|---|
| ORD ID | ord-b184b47f63ae4f6c94669374fdab15fc |
|---|
| Source note | uspto-grants-2003_05 |
|---|