HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 221969Generated: October 30, 2026
Hydrochloric Acid → HCID 59707070, compound
https://huagongshe.com/reaction/221969
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Hydroxy benzimidazole | HCID 11985 | — |
| Reactant | 4-Nitrobenzyl bromide | HCID 66011 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 59707070 | HCID 59707070 | 29.7% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08207182B2 |
|---|
| Source dataset | uspto-grants-2012_06 |
|---|
| ORD ID | ord-aba2624f2b12468594aee42485dc6b42 |
|---|
| Source note | uspto-grants-2012_06 |
|---|