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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2080628Generated: October 30, 2026

1-(5,6-dichloro-1H-benzoimidazol-2-yl)-2,2,2-trifluoro-ethanone → HCID 58333149, compound

https://huagongshe.com/reaction/2080628

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(5,6-dichloro-1H-benzoimidazol-2-yl)-2,2,2-trifluoro-ethanoneHCID 11594370—
ReactantHCID 178418797HCID 178418797—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
ProductHCID 58333149HCID 58333149—

Reaction Conditions

Temperature0 °C

Reaction Steps

To 1-(5,6-dichloro-1H-benzoimidazol-2-yl)-2,2,2-trifluoro-ethanone (595 mg) in THF (3 mL) at −78° C. was added 3-butenyl magnesium bromide (7.8 mL of 0.5 M in THF) dropwise. The resulting mixture was then stirred at 0° C. for 4 hr. The reaction was quenched with H2O and 1 N HCl, extracted with EtOAc, dried over Na2SO4, filtered, and concentrated to yield a residue. The residue was purified by flash chromatography with Biotage 40s+ column and elution with 10%-40% EtOAc/hexanes to yield a yellow solid. The yellow solid was dissolved in a minimal amount of Et2O and triturated with hexanes to yield the title compound as a tan solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07932399B2
Source datasetuspto-grants-2011_04
ORD IDord-5315684c27a24c3eb5ff5566111f5b32
Source noteuspto-grants-2011_04