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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2080621Generated: October 31, 2026

Iodine → HCID 44443105, compound

https://huagongshe.com/reaction/2080621

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
Reactant1-Propene, 1-bromo-, (1E)-HCID 639660—
ReactantMagnesiumHCID 5462224—
Reactant1-(5,6-dichloro-1H-benzoimidazol-2-yl)-2,2,2-trifluoro-ethanoneHCID 11594370—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
ProductHCID 44443105HCID 44443105—

Reaction Steps

To 1-(5,6-dichloro-1H-benzoimidazol-2-yl)-2,2,2-trifluoro-ethanone (636 mg) in THF (5 mL) at 0° C. was added Grignard reagent, which was freshly prepared from trans-1-bromo-1-propene (1.35 mL), a small iodine flake, and magnesium powder (382 mg) in THF (5 mL). The resulting mixture was then stirred at room temperature for 3 hr. The reaction was quenched with NH4Cl (sat. aq), filtered through a pad of Celite®, rinsed with EtOAc, the layers were separated, the aqueous layer 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 CH2Cl2 and triturated with hexanes to yield the title compound as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07932399B2
Source datasetuspto-grants-2011_04
ORD IDord-9bd1682514114094a313e03005693be5
Source noteuspto-grants-2011_04