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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 496264Generated: October 30, 2026

Triethylamine → 5-(3-Methoxyphenyl)benzimidazolidin-2-one

https://huagongshe.com/reaction/496264

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantN-methyl-2-pyrrolidoneHCID 13387—
Reactant4-Amino-3'-methoxy[1,1'-biphenyl]-3-carboxylic acidHCID 22325335—
Solvent1,4-DioxaneHCID 31275—
Product5-(3-Methoxyphenyl)benzimidazolidin-2-oneHCID 22325327—

Reaction Steps

To a suspension of 5-(3-methoxyphenyl)-2-aminobenzoic acid (2.0 g) in 1,4-dioxane (20 mL) add N-methylpyrolidinone (NMP, 5 mL) and triethylamine (1.4 mL), followed by diphenyl phosphoric azide (DPPA, 2.5 g). After stirring at ambient temperature for 30 minutes, heat the mixture to 100° C. for 2 hours, until gas evolution fully subsided. Cool the mixture to ambient temperature and concentrate in vacuo. Dissolve the residue in MeOH and leave to stand for 18 hours. Filter the precipitate and air dry to obtain 5-(3-methoxyphenyl)benzimidazolidin-2-one as a pale yellow solid. C. 2-Chloro-5-(3-methoxyphenyl)benzimidazole

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06943199B2
Source datasetuspto-grants-2005_09
ORD IDord-425a36a3b72d40c290f45ea2896389c4
Source noteuspto-grants-2005_09