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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 436101Generated: October 27, 2026

Ethanol → 1-Iodo-trans-1-octene-3-ol

https://huagongshe.com/reaction/436101

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantSodium borohydrideHCID 4311764—
Reactant(E)-1-Iodo-1-octen-3-oneHCID 11139597—
SolventWaterHCID 962—
Product1-Iodo-trans-1-octene-3-olHCID 11043283—

Reaction Steps

A solution of 78.2 g. (0.310 moles) of 1-iodo-trans-1-octen-3-one (Example 724) in 150 ml. of absolute ethanol is added dropwise over 2 hours to a slurry of 6.49 g. (0.172 moles) of sodium borohydride in 50 ml. of absolute ethanol cooled in an ice bath. After the addition is complete, the mixture is stirred for 2 hours with ice cooling and is then poured into 1 l. of water. The mixture is extracted into benzene and the organic phase is washed with saturated brine, dried (Na2SO4) and evaporated. The resulting oil is dissolved into 400 ml. of absolute ethanol and treated with 5 mole percent of p-carboxyphenylhydrazine at 70° C. for 1.5 hours to remove residual ketone. The mixture is cooled and evaporated and the residue is dissolved into 400 ml. of ether and is filtered. The filtrate is washed with dilute sodium bicarbonate solution and saturated brine, dried (Na2SO4), and evaporated to an oil. This oil is chromatographyed upon 2 Kg. of Florisil packed in hexane and the product is obtained upon elution with benzene Distillation of the product yields a colorless oil, b.p. 74°-76° C. (0.005 tor.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04007210
Source datasetuspto-grants-1977_02
ORD IDord-c4e4f79f7c7541d09589eaebed505d31
Source noteuspto-grants-1977_02