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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2420413Generated: October 29, 2026

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

https://huagongshe.com/reaction/2420413

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant1-Chloro-trans-1-octen-3-oneHCID 11041003—
Reactant1-Bromo-trans-1-octen-3-oneHCID 11790338—
SolventEthanolHCID 702—
Product1-Bromo-trans-1-octen-3-olHCID 13046280—

Reaction Steps

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04110368
Source datasetuspto-grants-1978_08
ORD IDord-a26ac1a9a7214360948410447f96e638
Source noteuspto-grants-1978_08