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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 221969Generated: October 30, 2026

Hydrochloric Acid → HCID 59707070, compound

https://huagongshe.com/reaction/221969

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium IodideHCID 4875—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Hydroxy benzimidazoleHCID 11985—
Reactant4-Nitrobenzyl bromideHCID 66011—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 59707070HCID 5970707029.7%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a solution of benzimidazolinone (1.5 g, 11.2 mmol) in abs. DMF (25 mL) there were added 4-nitrobenzyl bromide (2.16 g, 10 mmol), potassium carbonate (2.76 g, 20 mmol), and a catalytic amount of potassium iodide under a blanket of argon. The reaction mixture was heated to 100° C. over a period of 2 h. Following cooling, the reaction mixture was poured into a solution of H2O (200 mL) and 2N hydrochloric acid solution in H2O (10 mL). The resulting mixture was extracted with EtOAc (5×40 mL), the combined organic phases were washed with sat. NaCl solution (2×30 mL), dried over Na2SO4, and the solvent was removed in vacuo. The residue was taken up in hot toluene (100 mL), and the resulting solid matter was isolated by filtration. The filtrate was concentrated in vacuo. The residue was purified by means of column chromatography (SiO2, cyclohexane/EtOAc 1:1), and there were obtained 1,3-bis(4-nitrobenzyl)-1,3-dihydrobenzimidazol-2-one (W) (1.65 g, mp: 200-201° C.) and 1-(4-nitrobenzyl)-1,3-dihydrobenzimidazol-2-one (V) (600 mg, 22% of theory).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08207182B2
Source datasetuspto-grants-2012_06
ORD IDord-aba2624f2b12468594aee42485dc6b42
Source noteuspto-grants-2012_06