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HRID 2232614Erstellt: 24. Oktober 2026

Sodium Chloride → 6-bromo-hexahydro-3,5-methano-2H-cyclopenta[b]furan-2-ol

https://huagongshe.com/de/reaction/2232614

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium ChlorideHCID 5234—
Edukt6-Bromohexahydro-2h-3,5-methanocyclopenta[b]furan-2-oneHCID 263640—
EduktPotassium alloy, nonbase, K,NaHCID 16211683—
EduktDiisobutylaluminumhydrideHCID 21225700—
LösungsmittelTolueneHCID 1140—
Produkt6-bromo-hexahydro-3,5-methano-2H-cyclopenta[b]furan-2-olHCID 21284029103,1%

Reaktionsbedingungen

Temperatur-60 °C

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04788305
Quelldatensatzuspto-grants-1988_11
ORD IDord-dde02ce47971441ca5f40e50f5e460da
Quellennotizuspto-grants-1988_11