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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantAmmonium formateHCID 2723923—
Reactant1h-Benzimidazole-1-carboxylic acid,4-methyl-5-nitro-,1,1-dimethylethyl esterHCID 15896317—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product5-Amino-1-1-butoxycarbonyl-4-methylbenzimidazoleHCID 67788748—

Reaction Conditions

Temperature50 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05478858
Source datasetuspto-grants-1995_12
ORD IDord-bd7367dff5954afd98f94bebdb299711
Source noteuspto-grants-1995_12