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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 433009Generated: October 26, 2026

Allyl bromide → 1,3-Butadienylferrocene

https://huagongshe.com/reaction/433009

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantHexaneHCID 8058—
ReactantMagnesiumHCID 5462224—
ReactantFerrocenecarboxyaldehydeHCID 15184314—
SolventTetrahydrofuranHCID 8028—
Product1,3-ButadienylferroceneHCID 12966523284%

Reaction Steps

72 mg (3.0 mmole) of magnesium metal was placed in a 50 ml round bottom flask. 214 mg (1.0 mmole) of ferrocenaldehyde and 181.5 mg (1.5 mmole) of allyl bromide were dissolved in 15 ml of THF. The resulting mixture was poured into the round bottom flask containing the magnesium metal, while stirring at room temperature for two hours. After two-hour stirring, the cover of the flask was opened, and the liquid portion of the reaction mixture was introduced into a silica gel column, which had been wetted with n-hexane. All the liquid migrated into the silica gel, and the column was placed still for 24 hours. Next, the column was eluted with n-hexane. After evaporating the solvent from the eluate collected, 200 mg (0.84 mmole) of a purified title product was obtained with a yield of 84%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06664409B1
Source datasetuspto-grants-2003_12
ORD IDord-e0828d4510c64f71a754e5983a7caf60
Source noteuspto-grants-2003_12