HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 429550Generated: October 29, 2026
5-Nitrobenzimidazole → HCID 178441251, compound
https://huagongshe.com/reaction/429550
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 5-Nitrobenzimidazole | HCID 7195 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Product | HCID 178441251 | HCID 178441251 | — |
| Product | HCID 178441364 | HCID 178441364 | — |
Reaction Steps
To a solution of 5-nitrobenzimidazole (0.41 g, 2.5 mmol) was added a solution of n-BuLi (7.5 mmol) and reaction mixture was stirred for 1 h at 0° C. The reaction mixture was quenched by adding a few drops of H2O and concentrated in vacuo yielding an oil which was subjected to silica gel column chromatography (5% MeOHI EtOAC) to provide 0.13 g of 4-n-butyl-5-nitrobenzimidazole and 0.19 g of 4-n-butyl-5-aminobenzimidazole. The nitrobenzimidazole was converted to the amine in hydrogenation (H2/Pd—C) to provide 0.28 g,(1.5 mmol, 60%) of the desired product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06316637B1 |
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| Source dataset | uspto-grants-2001_11 |
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| ORD ID | ord-152b12e4addf4b02807de7e5cdbf0b13 |
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| Source note | uspto-grants-2001_11 |
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