HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium formate → 4,7-dimethyl-3H-benzimidazol-5-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium formate | HCID 2723923 | — |
| Reactant | 4,7-Dimethyl-5-nitro-1H-benzo[d]imidazole | HCID 22462221 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 4,7-dimethyl-3H-benzimidazol-5-amine | HCID 18379861 | — |
Reaction Steps
To a solution of 4,7-dimethyl-5-nitrobenzimidazole (1.17 g) in methanol (150 mL) is added Pd/C (10%, 0.16 g) and ammonium formate (1.31 g). The mixture is stirred at room temperature overnight, then filtered on Celite, with methanol wash of the solids. The filtrate is rotary evaporated and the residue partitioned between water and ethyl acetate. The organic layer is washed with saturated ammonium chloride, dried over magnesium sulfate, filtered and rotary evaporated to afford 5-amino-4,7-dimethylbenzimidazole as a foamy reddish solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05541210 |
| Source dataset | uspto-grants-1996_07 |
| ORD ID | ord-01043221d4e34bf18c6b48d65f791de2 |
| Source note | uspto-grants-1996_07 |