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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 906130Generated: October 31, 2026

Acetic Acid → methyl 1,4-dimethyl-1H-benzimidazole-5-carboxylate

https://huagongshe.com/reaction/906130

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantMethyl 2-methyl-4-(methylamino)-3-nitrobenzoateHCID 67403462—
CatalystPalladiumHCID 23938—
SolventEthyl AcetateHCID 8857—
Productmethyl 1,4-dimethyl-1H-benzimidazole-5-carboxylateHCID 6740521195.5%

Reaction Steps

A mixture of methyl 2-methyl-4-(methylamino)-3-nitrobenzoate (90 mg, 0.4 mmol), 10% palladium on charcoal (Degussa type, 90 mg), acetic acid (124 uL, 1.5 mmol), and ethyl acetate (20 mL) was shaken in a Parr hydrogenation apparatus at 40 psi for 18 hours. The reaction mixture was then filtered and concentrated. The residue was dissolved in formic acid was stirred at 100° C. for 1.5 hour. The reaction mixture was concentrated, quenched with ice-water (15 mL) and the pH was adjusted to basic by portion-wise sodium bicarbonate addition then extracted with ethyl acetate. The combined extract was washed with water (2×30 mL), brine (30 mL), dried over sodium sulfate, filtered and concentrated to give methyl 1,4-dimethyl-1H-benzimidazole-5-carboxylate (78 mg, 95% yield). MS (EI) for C 1H12N2O2: 205 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08012956B2
Source datasetuspto-grants-2011_09
ORD IDord-17a803b72fd4488997610bf16975d36b
Source noteuspto-grants-2011_09