HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Tetrahydrofuran → 4-n-Butylidene-4,5,6,7-tetrahydrobenzo[b]furan
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Tetrahydrofuran | HCID 8028 | — |
| Edukt | Ammonium Chloride | HCID 25517 | — |
| Edukt | 4,5,6,7-Tetrahydro-1-benzofuran-4-one | HCID 2733541 | — |
| Edukt | HCID 178418682 | HCID 178418682 | — |
| Lösungsmittel | Ethyl Acetate | HCID 8857 | — |
| Produkt | 4-n-Butylidene-4,5,6,7-tetrahydrobenzo[b]furan | HCID 54518756 | — |
Reaktionsschritte
To a mixture of 4-oxo-4,5,6,7-tetrahydrobenzo[b]furan (20.06 g) and THF (200 ml) was added dropwise 2M n-butylmagnesium bromide with ice-water cooling over 15 minutes. The mixture was stirred at r.t. overnight. The reaction mixture was poured into a mixture of a saturated aqueous solution of NH4Cl and AcOEt. The separated organic layer was washed with water and brine, and dried over MgSO4, and evaporated. The resulting oil was purified by chromatography on SiO2 (CHCl3 as eluent) to give 4-n-butylidene-4,5,6,7-tetrahydrobenzo[b]furan as a yellow oil (12.06 g).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US06274619B1 |
| Quelldatensatz | uspto-grants-2001_08 |
| ORD ID | ord-274df34808e2475186d75710ee35a1fe |
| Quellennotiz | uspto-grants-2001_08 |