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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 505913Generated: October 27, 2026

Hydrochloric Acid → Ethyl 2-(3-nitrophenyl)benzimidazole-4-carboxylate

https://huagongshe.com/reaction/505913

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant4-NitrobenzaldehydeHCID 541—
ReactantMethanolHCID 887—
ReactantEthyl 2,3-diaminobenzoateHCID 11171330—
ReactantSodium sulfide monohydrateHCID 19906495—
CatalystCupric acetateHCID 8895—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
ProductEthyl 2-(3-nitrophenyl)benzimidazole-4-carboxylateHCID 178468756—

Reaction Conditions

Temperature50 °C

Reaction Steps

4.2 g (23 mmol) of ethyl 2,3-diaminobenzoate and 3.1 ml of concentrated acetic acid were dissolved in 100 ml of methanol. 4.5 g (30 mmol) of 4-nitrobenzaldehyde, dissolved in 150 ml of methanol, were then added dropwise over a period of 30 minutes. 6 g (30 mmol) of copper(II) acetate, dissolved in 150 ml of warm water, were then rapidly added dropwise, and the entire mixture was subsequently refluxed for 20 minutes. The reaction solution was cooled to 50° C. and 8.3 ml of concentrated hydrochloric acid were added. This was followed by careful dropwise addition of a solution of 8.6 g of sodium sulfide hydrate in 100 ml of water, and the entire mixture was stirred for another 15 minutes. The reaction solution was poured into ice-water and the resulting precipitate was filtered off with suction. The filtrate was made alkaline using aqueous sodium bicarbonate solution and extracted repeatedly with ethyl acetate. The ethyl acetate phase was separated off, dried and concentrated under reduced pressure. This gave 6.1 g of the intermediate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07781596B1
Source datasetuspto-grants-2010_08
ORD IDord-51b9fa89093546a19c03d3fc93a99ece
Source noteuspto-grants-2010_08