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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2304707Generated: November 1, 2026

5-Nitrobenzimidazole → HCID 178439638, compound

https://huagongshe.com/reaction/2304707

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-NitrobenzimidazoleHCID 7195—
ReactantChloranilHCID 8371—
ReactantHCID 178455851HCID 178455851—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178439638HCID 17843963852%

Reaction Conditions

Temperature-15 °C

Reaction Steps

To a solution of 5-nitrobenzimidazole (2.3 g, 14 mmol) was added 14 ml of n-PrMgBr solution (42 mmol) and reaction mixture was stirred for 2 h at −15° C. The reaction was quenched by adding a solution of tetrachloro-1,4-benzoquinone (4 g, 16 mmol) in 10 ml of THF. The reaction mixture was concentrated in vacuo to provide an oil, which was subjected to column chromatographic separation (EtOAc, neat) to provide 1.4 g (7.2 mmol, 52%) of 4-n-propyl-5-nitrobenzimidazole, which was converted to the corresponding amine (1.2 g, >95%) by hydrogenation (H2, Pd/C).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06436982B1
Source datasetuspto-grants-2002_08
ORD IDord-d6173762fa09414398a4030fc2dc6285
Source noteuspto-grants-2002_08