HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 394872Erstellt: 25. Oktober 2026
Hexamethyldisilazane → 1-(4-Bromophenyl)-2-ethyl-4,4,4-trifluoro-1,3-butanedione
https://huagongshe.com/reaction/394872
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Hexamethyldisilazane | HCID 13838 | — |
| Edukt | 1-(Trifluoroacetyl)imidazole | HCID 73767 | — |
| Edukt | 1-Butanone, 1-(4-bromophenyl)- | HCID 78680 | — |
| Edukt | Butyllithium | HCID 178418339 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 1-(4-Bromophenyl)-2-ethyl-4,4,4-trifluoro-1,3-butanedione | HCID 22313809 | 69% |
Reaktionsschritte
To a solution of hexamethyldisilazane (4.92 g, 30.5 mmol) in THF (10 ml) was added dropwise n-BuLi (1.57 M hexane solution, 19.4 ml, 30.5 mmol) at −78° C. and the mixture was stirred at room temperature for 15 minutes. The mixture was cooled down to −78° C. again and 1-(4-bromophenyl)-1-butanone (5.77 g, 25.4 mmol) in THF (25 ml) was added dropwise over 15 min. The resulting mixture was stirred at −78° C. for 30 minutes, then allowed to warm up to 0° C. and stirred for 40 minutes. The solution was recooled down to −78° C. and N-trifluoroacetylimidazole (5.00 g, 30.5 mmol) was added. The mixture was stirred at −78° C. for 20 minutes, and at room temperature for 2 hours. The reaction was quenched with 2N HCl (30 ml). The organic layer was separated and the aqueous layer was extracted with ethyl acetate (50 ml×2). The combined organic layer was washed with brine (50 ml), dried over Na2SO4, and concentrated in vacuo. The residue was chromatographed over silica gel with hexane/ethyl acetate (8:1 to 3:1) to give 5.64 g (69%) of the title compound as a oil.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US06603008B1 |
|---|
| Quelldatensatz | uspto-grants-2003_08 |
|---|
| ORD ID | ord-4a5f9841b0274c38ae22e83dcd91db93 |
|---|
| Quellennotiz | uspto-grants-2003_08 |
|---|