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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2405051Generated: November 3, 2026

1-(5,6-dichloro-1H-benzoimidazol-2-yl)-2,2,2-trifluoro-ethanone → HCID 23729484, compound

https://huagongshe.com/reaction/2405051

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(5,6-dichloro-1H-benzoimidazol-2-yl)-2,2,2-trifluoro-ethanoneHCID 11594370—
ReactantHCID 178456138HCID 178456138—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
ProductHCID 23729484HCID 23729484—

Reaction Conditions

Temperature0 °C

Reaction Steps

To 1-(5,6-dichloro-1H-benzoimidazol-2-yl)-2,2,2-trifluoro-ethanone (793 mg) in THF (5 mL) at −78° C. was added isopropenyl magnesium bromide (12.3 mL of 0.5 M in THF) dropwise. The resulting mixture was then stirred at 0° C. for 5 hr. The reaction was quenched with H2O and 1 N HCl, extracted with EtOAc, dried over Na2SO4, filtered, and concentrated to a residue. The residue was purified by flash chromatography with Biotage 40s+ column and elution with 10%-40% EtOAc/hexanes to yield an orange gum. The orange gum was dissolved in a minimal amount of CH2Cl2 and triturated with hexanes to yield the title compound as a peach-colored solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08802865B2
Source datasetuspto-grants-2014_08
ORD IDord-1414d82895ad4c21ac580f74ea33dbd2
Source noteuspto-grants-2014_08