HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2273274Erstellt: 25. Oktober 2026
1-(5,6-dichloro-1H-benzoimidazol-2-yl)-2,2,2-trifluoro-ethanone → 2-(5,6-Dichloro-1H-benzoimidazol-2-yl)-1,1,1-trifluoro-pent-3-yn-2-ol
https://huagongshe.com/reaction/2273274
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | 1-(5,6-dichloro-1H-benzoimidazol-2-yl)-2,2,2-trifluoro-ethanone | HCID 11594370 | — |
| Edukt | HCID 178419101 | HCID 178419101 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 2-(5,6-Dichloro-1H-benzoimidazol-2-yl)-1,1,1-trifluoro-pent-3-yn-2-ol | HCID 23729188 | — |
Reaktionsschritte
To 1-(5,6-dichloro-1H-benzoimidazol-2-yl)-2,2,2-trifluoro-ethanone (535 mg) in THF (10 mL) at −78° C. was added 1-propynyl magnesium bromide (8 mL of 0.5 M in THF) dropwise. The resulting mixture was then stirred at 0° C. for 3 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 CH2Cl2 and triturated with hexanes to yield the title compound as a white solid.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09120830B2 |
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| Quelldatensatz | uspto-grants-2015_09 |
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| ORD ID | ord-1eba0f32a1b74d2fb913dcb16fd4ec1b |
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| Quellennotiz | uspto-grants-2015_09 |
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