HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 475187Generated: October 29, 2026
Ammonium formate → 4-Bromo-1H-benzimidazole
https://huagongshe.com/reaction/475187
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium formate | HCID 2723923 | — |
| Reactant | 3-Bromo-2-nitroaniline | HCID 21852072 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Formic Acid | HCID 284 | — |
| Product | 4-Bromo-1H-benzimidazole | HCID 11252584 | 30.5% |
Reaction Steps
To a mixture of 3-bromo-2-nitrobenzenamine (4.7 g, 21.66 mmol) in formic acid (98%, 50 mL) was added 10% Pd/C and ammonium formate (13.6 g, 216.6 mmol) and the reaction mixture was stirred under nitrogen at 120° C. for 24 h. The catalyst was filtered, the filtrate was concentrated, the residue was dissolved in water (100 mL) and extracted with EtOAc (2×150 mL). The combined organic extracts were washed with water and brine, dried (Na2SO4), filtered and concentrated in vacuo to afford 1.3 g (30%) of crude 4-bromo-1H-benzo[d]imidazole (52) as dark brown solid: MS (ESI) m/z=197.1 [M+1]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08637537B2 |
|---|
| Source dataset | uspto-grants-2014_01 |
|---|
| ORD ID | ord-2014d393f39a43559259cebf79fafcdf |
|---|
| Source note | uspto-grants-2014_01 |
|---|