Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1515034Generated: October 26, 2026

Ethyl Acetate → methyl (E)-3-{4-[6-(4-tert-butylphenylcarbamoyl)-1H-benzimidazol-2-yl]-3,5-dimethylphenyl}-acrylate

https://huagongshe.com/reaction/1515034

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantPotassium hydroxy sulfiteHCID 23707502—
ReactantMethyl 3-(3,5-dimethyl-4-formylphenyl)propionateHCID 54209618—
Reactant3,4-diamino-N-(4-tert-butylphenyl)-benzamideHCID 66966111—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Productmethyl (E)-3-{4-[6-(4-tert-butylphenylcarbamoyl)-1H-benzimidazol-2-yl]-3,5-dimethylphenyl}-acrylateHCID 66965696—

Reaction Steps

To a solution of 3,4-diamino-N-(4-tert-butylphenyl)-benzamide (1.83 g, 6.46 mmol) and 3-(4-formyl-3,5-dimethylphenyl)-propionic acid methyl ester (1.55 g, 7.10 mmol) (from Example 6-17) in DMF (25 mL) and water (2.5 mL) was added oxone (2.66 g, 4.33 mmols) and the mixture was stirred at ambient temperature for 1 h. The mixture was poured into ethyl acetate, extracted once with water and five times with brine, and the organic layer was dried, filtered, and the solvent was removed under reduced pressure. The residue was chromatographed using a 50-90% gradient of heptane/ethyl acetate to give methyl (E)-3-{4-[6-(4-tert-butylphenylcarbamoyl)-1H-benzimidazol-2-yl]-3,5-dimethylphenyl}-acrylate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08222248B2
Source datasetuspto-grants-2012_07
ORD IDord-a1fadefcde8b4177ba9baa7dd6272e22
Source noteuspto-grants-2012_07