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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 586443Generated: October 30, 2026

Benzoyl chloride → HCID 9864577, compound

https://huagongshe.com/reaction/586443

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
ReactantAmmonium thiocyanateHCID 15666—
ReactantHCID 22335511HCID 22335511—
SolventAcetoneHCID 180—
ProductHCID 9864577HCID 9864577—

Reaction Conditions

Temperature80 °C

Reaction Steps

Benzoylchloride (0.067 mol) was added to a solution of NH4SCN (5.09 g) in 2-propanone (150 ml) and the mixture was stirred and refluxed for 20 minutes. A solution of 4-[1-(1H-imidazol-1-yl)-2-methylpropyl]benzenamine (0.0557 mol) in 2-propanone (150 ml) was added and the mixture was stirred and refluxed at 80° C. overnight. The mixture was cooled, filtered through celite and the filtrate was evaporated. The residue was taken up in CH2Cl2. The organic layer was dried, filtered and the solvent evaporated. The residue was purified by column chromatography over silica gel (eluent: CH2Cl2/CH3OH/NH4OH 98/2/0.1). The pure fractions were collected and evaporated. The residue was recrystallized from 2-propanone and DIPE, yielding (±)-N-benzoyl-N′-[4-[1-(1H-imidazol-1-yl)-2-methylpropyl]phenyl]thiourea (compound 698).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06936626B2
Source datasetuspto-grants-2005_08
ORD IDord-05cd789c485b4334bc8c68df79efa76c
Source noteuspto-grants-2005_08