HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2273277Generated: October 30, 2026
3-Bromo-2-methyl-1-propene → HCID 23729502, compound
https://huagongshe.com/reaction/2273277
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Bromo-2-methyl-1-propene | HCID 357785 | — |
| Reactant | Indium | HCID 5359967 | — |
| Reactant | 1-(5,6-dichloro-1H-benzoimidazol-2-yl)-2,2,2-trifluoro-ethanone | HCID 11594370 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 23729502 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09120830B2 |
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| Source dataset | uspto-grants-2015_09 |
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| ORD ID | ord-fea109ab07d54c8a9b58af5bc0995913 |
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| Source note | uspto-grants-2015_09 |
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