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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 436095Erstellt: 25. Oktober 2026

Sodium borohydride → 1-Bromo-trans-1-octen-3-ol

https://huagongshe.com/reaction/436095

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium borohydrideHCID 4311764—
Edukt1-Chloro-trans-1-octen-3-oneHCID 11041003—
Edukt1-Bromo-trans-1-octen-3-oneHCID 11790338—
LösungsmittelEthanolHCID 702—
Produkt1-Bromo-trans-1-octen-3-olHCID 13046280—

Reaktionsschritte

To an ice cooled mixture of 14.29 g. (0.378 mole) of sodium borohydride in 400 ml. of anhydrous ethanol is added the crude 1-bromo-trans-1-octen-3-one (Example 725), from 0.424 mole of 1-chloro-trans-1-octen-3-one) over 30 minutes. The mixture is stirred for 2 hours with ice cooling and is then partitioned between ice water and benzene. The organic phase is washed with water and saturated brine, dried (Na2SO4), and evaporated to an oil. Fractional distillation yields the title compound as a colorless oil, b.p. 66°-68° C. (0.025 torr).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04007210
Quelldatensatzuspto-grants-1977_02
ORD IDord-d830b352695445648c9953de14021ee6
Quellennotizuspto-grants-1977_02