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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1258936Generated: November 4, 2026

Ethyl orthoformate → ethyl 3-benzyl-3H-benzo[d]imidazole-5-carboxylate

https://huagongshe.com/reaction/1258936

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl orthoformateHCID 31214—
ReactantEthyl 4-amino-3-(benzylamino)benzoateHCID 58213838—
CatalystHydrochloric AcidHCID 313—
SolventEthanolHCID 702—
Productethyl 3-benzyl-3H-benzo[d]imidazole-5-carboxylateHCID 5821380848.1%

Reaction Steps

A solution of ethyl 4-amino-3-(benzylamino)benzoate (0.24 g, 0.89 mmol) and triethyl orthoformate (0.8 mL, 4.8 mmol) in ethanol (10 mL) and conc. HCl (7 drops) was heated to reflux for 24 hr. The solution was cooled to room temperature and concentrated, then diluted with ethyl acetate (100 mL) and washed with dilute aq. NaHCO3 (1×100 mL). Then organic layer was dried (MgSO4), filtered and then concentrated and the resulting residue was purified by flash chromatography (50% ethyl acetate/hexane then ethyl acetate) to provide 0.12 g (48%) of ethyl 3-benzyl-3H-benzo[d]imidazole-5-carboxylate as an off white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08466193B2
Source datasetuspto-grants-2013_06
ORD IDord-36b8e473d8514497af10cbc53656e405
Source noteuspto-grants-2013_06