Cyclobutadieneiron tricarbonyl
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| Identifiers | |
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| Properties | |
| (C4H4)Fe(CO)3 | |
| Appearance | yellow solid |
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Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Cyclobutadieneiron tricarbonyl or (C4H4)Fe(CO)3 is an organoiron compound with the formula Fe(C4H4)(CO)3. It is a yellow solid that is soluble in organic solvents. It has been used in organic chemistry as a precursor for cyclobutadiene, which is an elusive species in the free state.
It was first prepared in 1965 by Rowland Pettit starting from cyclooctatetraene:
Cyclooctatetraene is chlorinated to the [4.2.0]-bicyclic compound which reacts further with the alkyne dimethyl acetylenedicarboxylate in a Diels-Alder reaction followed by a reverse-DA reaction by pyrolysis at 200 °C releasing cis-dichlorocyclobutene. This compound reacts with di-iron nonacarbonyl (obtained from photolysis of iron pentacarbonyl) to give cyclobutadieneiron tricarbonyl.
The compound is a half sandwich complex. The C-C distances are 1.426 Â.
Cyclobutadieneiron tricarbonyl displays aromaticity as evidenced by some of its reactions, which can be classified as electrophilic aromatic substitution:
It undergoes Friedel-Crafts acylation with acetyl chloride and aluminium chloride to give the acyl derivative 2, with formaldehyde and hydrochloric acid to the chloromethyl derivative 3, in a Vilsmeier-Haack reaction with N-methylformanilide and phosphorus oxychloride to the formyl 4, and in a Mannich reaction to amine derivative 5.
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