Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2188810Generated: November 2, 2026

Ethanol → HCID 58993777, compound

https://huagongshe.com/reaction/2188810

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantLithium HydroxideHCID 3939—
ReactantEthyl AcetateHCID 8857—
ReactantHCID 178487288HCID 178487288—
SolventWaterHCID 962—
ProductHCID 58993777HCID 5899377729%

Reaction Steps

Into a 50 mL round bottom flask was placed (E)-2-bromo-N-[1-(2-bromo-benzoyl)-5-(5-methoxy-2-trifluoromethyl-benzoimidazol-1-yl)-1H-pyrazin-2-ylidene]-benzamide (vi) (50 mg, 0.07 mmol). To this was added LiOH (100 mg), followed by EtOH (25 mL). The resulting solution was allowed to react, with stirring, for 30 minutes while the temperature was maintained at room temperature. The reaction progress was monitored by TLC (EtOAc/PE=1:2). After completion, the resulting solution was diluted with 15 mL of H2O and extracted two times with 10 mL of EtOAc. The organic layers were combined and dried over Na2SO4. After removal of the solvent and volatile components under vacuum, the residue was purified by eluting through a silica gel column with a 1:6 EtOAc/PE solvent system. This resulted in 10 mg (27%) of the final product 2-bromo-N-[5-(5-methoxy-2-trifluoromethyl-benzoimidazol-1-yl)-pyrazin-2-yl]-benzamide as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08324219B2
Source datasetuspto-grants-2012_12
ORD IDord-0246b56a4db348db99e6cbae136d3fa5
Source noteuspto-grants-2012_12