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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2399691Generated: November 1, 2026

Sodium Iodide → 11-Iodoundec-1-ene

https://huagongshe.com/reaction/2399691

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantTriethylamineHCID 8471—
Reactant11-Iodoundec-1-eneHCID 11119462—
SolventAcetoneHCID 180—
SolventMethyl Ethyl KetoneHCID 6569—
Product11-Iodoundec-1-eneHCID 11119462—
ProductHCID 85678669HCID 85678669—

Reaction Steps

Polyalkylenes, which are available, can be prepared by polymerization of olefins, especially the 1-olefins such as 1-butene, 1-pentene, undecylenic acid-trimethylsilyl ester, and the like, using an isotactic catalyst, especially TiCl3AA/diethylaluminum chloride in toluene. Undecylenic acid-trimethylsilyl ester was, for example, prepared from the reaction of undecylenic acid with trimethylsilyl chloride; undecylenyl iodide was prepared from undecylenol; and undecylenol was allowed to react with thionyl chloride and pyridine to form undecylenyl chloride which was then converted to undecylenyl iodide by reaction with sodium iodide in acetone or methyl ethyl ketone. Undecylenyl triethylammonium iodide was formed by the reaction of undecylenyl iodide and triethylamine in alcohol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05451483
Source datasetuspto-grants-1995_09
ORD IDord-08b761836f484b698422a041725aa9b1
Source noteuspto-grants-1995_09