HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 256230Erstellt: 26. Oktober 2026
Sodium Chloride → 6-bromo-hexahydro-3,5-methano-2H-cyclopenta[b]furan-2-ol
https://huagongshe.com/reaction/256230
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Sodium Chloride | HCID 5234 | — |
| Edukt | 6-Bromohexahydro-2h-3,5-methanocyclopenta[b]furan-2-one | HCID 263640 | — |
| Edukt | Potassium alloy, nonbase, K,Na | HCID 16211683 | — |
| Edukt | Diisobutylaluminumhydride | HCID 21225700 | — |
| Lösungsmittel | Toluene | HCID 1140 | — |
| Produkt | 6-bromo-hexahydro-3,5-methano-2H-cyclopenta[b]furan-2-ol | HCID 21284029 | 103,1% |
Reaktionsschritte
275 ml of a toluene solution of 1.2M of diisobutyl aluminium hydride were slowly added at -60° C. to a mixture of 62.16 g of 6-bromo-hexahydro-3,5-methano-2H-cyclopenta[b]furan-2-one [prepared by method of Ver Nooy et al, J.A.C.S., Vol. 77 (1955), p. 3583] and 500 ml of toluene and the mixture was stirred at -60° C. for 45 minutes and was then poured into aqueous 1M sodium potassium double tartrate. The mixture was stirred for 2 hours and the decanted aqueous phase was saturated with sodium chloride and extracted with methylene chloride. The combined organic phases were evaporated to dryness under reduced pressure to obtain 64.7 g of racemic 6-bromo-hexahydro-3,5-methano-2H-cyclopenta[b]furan-2-ol melting at 104° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US04701542 |
|---|
| Quelldatensatz | uspto-grants-1987_10 |
|---|
| ORD ID | ord-224054a31a66430e9a4abad27f4d8b51 |
|---|
| Quellennotiz | uspto-grants-1987_10 |
|---|