HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Pentyltriphenylphosphonium bromide → (Butylmethylene)triphenylphosphorane
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Pentyltriphenylphosphonium bromide | HCID 2724565 | — |
| Edukt | Potassium bis(trimethylsilyl)amide | HCID 3251421 | — |
| Edukt | 1-(3,5-Dimethoxyphenyl)-1-(hex-1-enyl)-cyclopentane | HCID 69204664 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | (Butylmethylene)triphenylphosphorane | HCID 10980496 | — |
Reaktionsbedingungen
| Temperatur | 10 °C |
|---|
Reaktionsschritte
To a suspension of pentyltriphenylphosphonium bromide (5 equiv.) in dry THF (0.18M) at 0° C., under an argon atmosphere was added potassium bis(trimethylsilyl) amide (4.9 equiv.). The mixture was warmed to 10° C. and stirred for an additional 30 min to ensure complete formation of the orange ylide. The resulting slurry was used in the preparation of 1-(3,5-dimethoxyphenyl)-1-(hex-1-enyl)-cyclopentane.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US07285683B2 |
| Quelldatensatz | uspto-grants-2007_10 |
| ORD ID | ord-5608aedb77d3428e9e4779505b624f9e |
| Quellennotiz | uspto-grants-2007_10 |