HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2273276Generated: October 30, 2026
1-(5,6-dichloro-1H-benzoimidazol-2-yl)-2,2,2-trifluoro-ethanone → HCID 23729481, compound
https://huagongshe.com/reaction/2273276
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-(5,6-dichloro-1H-benzoimidazol-2-yl)-2,2,2-trifluoro-ethanone | HCID 11594370 | — |
| Reactant | HCID 178418255 | HCID 178418255 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 23729481 | HCID 23729481 | — |
Reaction Steps
To 1-(5,6-dichloro-1H-benzoimidazol-2-yl)-2,2,2-trifluoro-ethanone (595 mg) in THF (5 mL) at −78° C. was added phenyl magnesium bromide (4.6 mL of 1 M in THF) dropwise. The resulting mixture was 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 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 tan 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-70887b0647464ca886ab9ddd8a5da4fd |
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| Source note | uspto-grants-2015_09 |
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