HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2260723Generated: October 30, 2026
Ethyl Acetate → 5-Amino-1-1-butoxycarbonyl-4-methylbenzimidazole
https://huagongshe.com/reaction/2260723
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Ammonium formate | HCID 2723923 | — |
| Reactant | 1h-Benzimidazole-1-carboxylic acid,4-methyl-5-nitro-,1,1-dimethylethyl ester | HCID 15896317 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 5-Amino-1-1-butoxycarbonyl-4-methylbenzimidazole | HCID 67788748 | — |
Reaction Steps
To a solution of 1-tert-butoxycarbonyl-4-methyl-5-nitrobenzimidazole (8 g) in methanol (40 mL)/ethyl acetate (400 mL) is added palladium-on-carbon (Pd/C) (10%, 0.5 g) and ammonium formate (7.27g). The mixture is stirred at 50° C. for 2 hours, 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 pure 5-amino-1-1-butoxycarbonyl-4-methylbenzimidazole as an off-white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05478858 |
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| Source dataset | uspto-grants-1995_12 |
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| ORD ID | ord-bd7367dff5954afd98f94bebdb299711 |
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| Source note | uspto-grants-1995_12 |
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