HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
3-Bromobenzaldehyde → 1-Bromo-3-(2-methyl-1-propenyl)benzene
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | 3-Bromobenzaldehyde | HCID 76583 | — |
| Edukt | Isopropyltriphenylphosphonium iodide | HCID 2723783 | — |
| Edukt | Potassium tert-butoxide | HCID 23665647 | — |
| Katalysator | 18-Crown-6 | HCID 28557 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 1-Bromo-3-(2-methyl-1-propenyl)benzene | HCID 21706836 | 75,3% |
Reaktionsschritte
To a stirred slurry of 17.83 g (41.2 mmol) of isopropyltriphenylphosphonium iodide and 300 mg (1.1 mmol) of 18-crown-6 in 50 mL of THF under nitrogen at 5° C. was added 4.60 g (41.0 mmol) of potassium t-butoxide over 5 minutes. The resulting deep red-orange slurry was stirred 10 minutes and then a solution of 4.31 mL (37.0 mmol) of 3-bromobenzaldehyde in 40 mL of THF was added at a rate to keep the temperature below 10° C. The resulting bright yellow slurry was stirred for 20 minutes and then poured into 300 mL of hexanes. The solids were filtered off and the filtrate evaporated. This residue was purified by flash chromatography (5×15 cm column) and eluted with hexanes to provide 5.88 g (75%) of title compound as a colorless oil.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US05157027 |
| Quelldatensatz | uspto-grants-1992_10 |
| ORD ID | ord-2e4bd4a7bf1b4401a81feba32fb102f2 |
| Quellennotiz | uspto-grants-1992_10 |