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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 413730Generated: October 30, 2026

Phenyl Isothiocyanate → HCID 18521791, compound

https://huagongshe.com/reaction/413730

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenyl IsothiocyanateHCID 7673—
ReactantCyanamideHCID 9864—
Reactant2-Bromo-1-(3-nitrophenyl)ethan-1-oneHCID 75213—
ReactantSodiumHCID 5360545—
SolventMethanolHCID 887—
SolventWaterHCID 962—
ProductHCID 18521791HCID 1852179177.8%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06569878B1
Source datasetuspto-grants-2003_05
ORD IDord-b184b47f63ae4f6c94669374fdab15fc
Source noteuspto-grants-2003_05