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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2405053Generated: November 1, 2026

3-Bromo-2-methyl-1-propene → HCID 23729502, compound

https://huagongshe.com/reaction/2405053

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Bromo-2-methyl-1-propeneHCID 357785—
ReactantIndiumHCID 5359967—
Reactant1-(5,6-dichloro-1H-benzoimidazol-2-yl)-2,2,2-trifluoro-ethanoneHCID 11594370—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
ProductHCID 23729502HCID 23729502—

Reaction Steps

To 1-(5,6-dichloro-1H-benzoimidazol-2-yl)-2,2,2-trifluoro-ethanone (609 mg) in THF (4 mL) and H2O (12 mL) at room temperature were added 3-bromo-2-methyl-propene (0.31 mL), followed by indium powder (279 mg, −100 mesh). The resulting mixture was then stirred at room temperature for 18 hr. The resulting mixture was filtered through a pad of Celite®, rinsed with EtOAc, the layers 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 an orange gum. The orange gum was dissolved in a minimal amount of CH2Cl2 and triturated with hexanes to yield the title compound as an orange solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08802865B2
Source datasetuspto-grants-2014_08
ORD IDord-7ed08f85321e408e96d36ea69f2221c7
Source noteuspto-grants-2014_08