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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1903968Generated: November 2, 2026

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

https://huagongshe.com/reaction/1903968

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 numberUS04439365
Source datasetuspto-grants-1984_03
ORD IDord-9e76bcdf16eb4602b11f337fa3b103d0
Source noteuspto-grants-1984_03