HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
2'-Bromoacetophenone → 1-Bromo-2-(prop-1-en-2-yl)benzene
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | 2'-Bromoacetophenone | HCID 75060 | — |
| Edukt | Potassium tert-butoxide | HCID 23665647 | — |
| Katalysator | Methyltriphenyliphosphonium bromide | HCID 74505 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 1-Bromo-2-(prop-1-en-2-yl)benzene | HCID 12486618 | 88% |
Reaktionsschritte
To a suspension of methyltriphenyl phosphonium bromide (108 g, 303 mmol) in THF (750 mL) at room temperature was added KOtBu (112.24 g, 303 mmol) in portions. After being stirred for 5 min, the reaction mixture was treated with 2′bromoacetophenone (50.3 g, 253 mmol). The reaction mixture was stirred for 3 hrs at room temperature then quenched with saturated ammonium chloride. Extracted 3× with Et2O and the combined organic layers were washed with brine, dried over MgSO4 and evaporated under vacuum. Purified by silica gel chromatography (100% petroleum ether) to give 43.8 g (88%) of 1-bromo-2-(prop-1-en-2-yl)benzene as a colorless oil.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US08895534B2 |
| Quelldatensatz | uspto-grants-2014_11 |
| ORD ID | ord-aca79341b3294c7c989a73bcd4f9138b |
| Quellennotiz | uspto-grants-2014_11 |