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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 322846Generated: October 25, 2026

Allyl bromide → Phenyl-ferrocenyl-butadien

https://huagongshe.com/reaction/322846

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
Reactant1,2-DiiodoethaneHCID 12224—
ReactantSamariumHCID 23951—
ReactantCyclopenta-1,3-diene;cyclopenta-2,4-dien-1-yl(phenyl)methanone;iron(2+)HCID 176468997—
ReactantHCID 178506586HCID 178506586—
SolventTetrahydrofuranHCID 8028—
ProductPhenyl-ferrocenyl-butadienHCID 12962983299%

Reaction Steps

In a nitrogen environment, about 330 mg (2.20 mmole) of samarium and about 500 mg (1.77 mmole) of 1,2-diiodoethane is disposed in a round-bottomed flask. About 20 ml of tetrahydrofuran is added into the round-bottomed flask. The mixture in the round-bottomed flask is stirred until a deep-blue samarium diiodide solution is obtained. Following the process flow described in Example 1, about 348 mg (1.20 mmole) of benzoylferrocene reacts with about 242 mg (2.0 mmole) of allyl bromide to produce oil-type 1-Ferrocenyl-1-phenyl-1,3-butadiene (3c) with a weight of about 373 mg (1.19 mmole) and a yield of about 99%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06211392B1
Source datasetuspto-grants-2001_04
ORD IDord-bbdbdb3bbb01451496fa2ee7abb17493
Source noteuspto-grants-2001_04