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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Methyl 2-methyl-4-(methylamino)-3-nitrobenzoate | HCID 67403462 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | methyl 1,4-dimethyl-1H-benzimidazole-5-carboxylate | HCID 67405211 | 95.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08012956B2 |
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| Source dataset | uspto-grants-2011_09 |
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| ORD ID | ord-17a803b72fd4488997610bf16975d36b |
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| Source note | uspto-grants-2011_09 |
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