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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1112678Generated: October 27, 2026

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

https://huagongshe.com/reaction/1112678

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 numberUS04123456
Source datasetuspto-grants-1978_10
ORD IDord-b2a8681bb81a429da02854e5a8a502ff
Source noteuspto-grants-1978_10