HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 396737Erstellt: 23. Oktober 2026
Ethyl trifluoroacetate → Butane-1,3-dione, 4,4,4-trifluoro-1-(4-imidazol-1-ylphenyl)-
https://huagongshe.com/de/reaction/396737
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Ethyl trifluoroacetate | HCID 9794 | — |
| Edukt | Hexamethyldisilazane | HCID 13838 | — |
| Edukt | 1-(4-(1H-Imidazol-1-yl)phenyl)ethanone | HCID 82316 | — |
| Edukt | Butyllithium | HCID 178418339 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | Butane-1,3-dione, 4,4,4-trifluoro-1-(4-imidazol-1-ylphenyl)- | HCID 6426099 | — |
Reaktionsschritte
To a THF (5 mL) solution of 1,1,1,3,3,3-hexamethyldisilazane (0.178 g, 1.1 mmol) was added n-butyl lithum (1.6 M solution in hexane, 0.72 mL, 1.2mmol) at 0° C. under nitrogen, and the mixture was stirred for 30 minutes, and cooled to −78° C. 4-(1-Imidazolyl)acetophenone (prepared according the method of M. A. Khan et, al., J. Chem. Soc. C., 1970, 85., 0.186 g, 1.0 mmol) was added to the mixture, and residue was stirred for 1 hour. Ethyl trifluoroacetate (0.17 g, 1.2 mmol) was added tothe reaction mixture, the residure was warm to room temperature. The reaction mixture was poured into ice water and the whole was extracted with ethyl acetate (30 mL×2). The organic layer was washed with brine, dried over Na2SO4, and concentrated in vacuo. The resulting solid was washed with small amount of ethyl acetate to give the title compound (0.163 g).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06608095B2 |
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| Quelldatensatz | uspto-grants-2003_08 |
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| ORD ID | ord-014edeebc2ec4087a1b941830e15dd7f |
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| Quellennotiz | uspto-grants-2003_08 |
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