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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 475187Generated: October 29, 2026

Ammonium formate → 4-Bromo-1H-benzimidazole

https://huagongshe.com/reaction/475187

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium formateHCID 2723923—
Reactant3-Bromo-2-nitroanilineHCID 21852072—
CatalystPalladiumHCID 23938—
SolventFormic AcidHCID 284—
Product4-Bromo-1H-benzimidazoleHCID 1125258430.5%

Reaction Conditions

Temperature120 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08637537B2
Source datasetuspto-grants-2014_01
ORD IDord-2014d393f39a43559259cebf79fafcdf
Source noteuspto-grants-2014_01