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Original Articles

The Synthesis of 1,1′-Ferrocenyldiamines

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Pages 321-330 | Received 07 Sep 1982, Accepted 07 Dec 1982, Published online: 05 Dec 2006

References

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  • Continued bubbling after initial saturation leads to the formation of tarry residues. This is more apparent using α-hydroxethyl ferrocenes
  • A chilled sample of neat dimethylamine was used in this preparation, however, satisfactory results may be achieved using a 40% aqueous solution of dimethylamine
  • When an aqueous solution of the amine was used no precipitate was observed. The benzene solution was separated, dried over anhydrous MgSO4, and its solvent volume reduced to a few mLs. prior to column chromatography. Product yields were not diminished when aqueous amines were used
  • Oil crystallised on standing for 1–2 weeks

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