HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1414376Generated: November 2, 2026
Hydrochloric Acid → 2-[p-Carboxyphenyl]-5,6-diaminobenzimidazole hydrochloride
https://huagongshe.com/reaction/1414376
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Reactant | HCID 178524232 | HCID 178524232 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2-[p-Carboxyphenyl]-5,6-diaminobenzimidazole hydrochloride | HCID 21487213 | 82% |
Reaction Steps
A solution of 5 g (16.7 mmole) of 2-[p-carboxyphenyl]-5,6-dinitrobenzimidazole (as prepared in Example I) in 200 ml of methanol at 0° C was thoroughly purged with nitrogen. To this was added 500 mg of 10% palladium on charcoal, and 30 ml of concentrated HCl. The hydrogenation flask was then pressurized with 55 lbs/in2 of hydrogen, and the flask was shaken at room temperature for 8 hours. After the reaction period had elapsed, the solution was filtered by suction, and the filtrate evaporated to dryness in vacuo. The residual yellow solid was redissolved in a minimum amount of boiling methanol (which contained a trace of HCl), and the filtered solution added to 50 ml of concentrated HCl. Removal of the methanol from the solution in vacuo and subsequent cooling in ice yielded 4.2 g (82%) of 2-[p-carboxyphenyl]-5,6-diaminobenzimidazole hydrochloride as fluffy yellow needles.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04001268 |
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| Source dataset | uspto-grants-1977_01 |
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| ORD ID | ord-b0d247dfd38644deaceefc02493dc571 |
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| Source note | uspto-grants-1977_01 |
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