Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 433007Generated: October 26, 2026

Allyl bromide → 1,3-Butadienylferrocene

https://huagongshe.com/reaction/433007

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantFerrocenecarboxyaldehydeHCID 15184314—
ReactantHCID 178450094HCID 178450094—
ReactantHCID 178466060HCID 178466060—
CatalystMagnesiumHCID 5462224—
SolventDiethyl EtherHCID 3283—
Product1,3-ButadienylferroceneHCID 129665232—

Reaction Steps

Ferrocenaldehyde or ferrocenyl methyl ketone and allyl bromide are reacted in an ether solvent and in the presence of magnesium metal as a catalyst. The liquid portion of the reaction mixture is introduced into a silica gel column, wherein the weak acidity of the silica gel is able to dehydrate the reaction intermediate 1-ferrocenyl-3-buten-1-ol product. The column is eluted with n-hexane, and after evaporating the solvent from the eluate collected, a purified ferrocenyl-1,3-butadiene product is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06664409B1
Source datasetuspto-grants-2003_12
ORD IDord-1873e47b27344b03a5faf5cb04c75af6
Source noteuspto-grants-2003_12