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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1400664Generated: October 30, 2026

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

https://huagongshe.com/reaction/1400664

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 numberUS08906954B2
Source datasetuspto-grants-2014_12
ORD IDord-4246395bea3945119a2cfce70560035f
Source noteuspto-grants-2014_12