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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1736462Generated: October 30, 2026

Ammonium formate → 4,7-dimethyl-3H-benzimidazol-5-amine

https://huagongshe.com/reaction/1736462

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium formateHCID 2723923—
Reactant4,7-Dimethyl-5-nitro-1H-benzo[d]imidazoleHCID 22462221—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product4,7-dimethyl-3H-benzimidazol-5-amineHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05541210
Source datasetuspto-grants-1996_07
ORD IDord-01043221d4e34bf18c6b48d65f791de2
Source noteuspto-grants-1996_07