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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1828657Generated: October 31, 2026

Bis(eta-cyclopentadienyl) iron → HCID 178424122, compound

https://huagongshe.com/reaction/1828657

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBis(eta-cyclopentadienyl) ironHCID 7611—
ReactantN,N,N',N'-TetramethylethylenediamineHCID 8037—
ReactantDimesitylboron fluorideHCID 3466040—
ReactantButyllithiumHCID 178418339—
SolventHexaneHCID 8058—
ProductHCID 178424122HCID 178424122—

Reaction Steps

15.4 ml (24.7 mmol) of a 1.6 M solution of n-butyllithium in n-hexane were added dropwise to a mixture of 2.87 g=3.7 ml (24.7 mmol) of N,N,N′,N′-tetramethylethylenediamine and 4 ml of n-hexane over a period of 5 minutes while stirring at room temperature. The reaction mixture was stirred for another 20 minutes at room temperature and a solution of 1.86 g (10 mmol) of ferrocene in 70 ml of n-hexane was then added dropwise over a period of 25 minutes. The reaction mixture was stirred at room temperature for 6 hours and a solution of 6.62 g (24.7 mmol) of fluorodimesitylborane in n-hexane was then added dropwise over a period of 30 minutes. After stirring at room temperature for 16 hours the n-hexane was removed on a rotary evaporator, the red, semisolid residue was taken up in 400 ml of dichloromethane, the organic phase was admixed with 3 ml of water, stirred vigorously for 30 minutes and subsequently dried over magnesium sulfate. After the desiccant had been filtered off, the organic phase was evaporated to dryness. The red crude product (about 6.8 g, purity according to HPLC: 95–98%) was stirred once with hot n-hexane and subsequently recrystallized from ethanol until a purity of 99.8% as determined by HPLC had been reached. The yield, at a purity of 99.8% as determined by HPLC, was 4.7 g, corresponding to 68.8%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07060369B2
Source datasetuspto-grants-2006_06
ORD IDord-95753b0e478444eb85451603c6e50300
Source noteuspto-grants-2006_06