reaction mechanism acetylation ferrocene


How is ferrocene acylated?

    In this experiment, ferrocene is acylated using acetic anhydride with a catalytic amount of phosphoric acid. There are two possible products, acetylferrocene and 1,1’-diacetylferrocene, which will be identified at the end of this reaction.

Can ferrocene undergo electrophilic aromatic substitution?

    The reactivity of ferrocene is similar to other aromatic compounds. Therefore, it can undergo electrophilic aromatic substitution ina very similar mechanism to that of benzene. In this experiment, ferrocene is acylated using acetic anhydride with a catalytic amount of phosphoric acid.

What is the difference between Friedel-Crafts acylation of benzene and ferrocene?

    Thus, while the Friedel-Crafts acylation of benzene requires aluminum chloride as a catalyst, ferrocene can be acylated by acetic anhydride under milder conditions using phosphoric acid as the catalyst. In addition, the second ring may also be acetylated to give 1,1'-diacetylferrocene, Fe(C5H4COCH3)2.

How do you mix phosphoric acid and ferrocene?

    Phosphoric acid can cause serious burns, particularly to the eyes; do not allow it to contact your eyes, skin or clothing. Place 0.28 g of ferrocene in the dry reaction tube. Using the markings on the reaction tube, add 1.0 mL of acetic anhydride to the ferrocene.
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reaction mechanism for alkaline hydrolysis of tert butyl bromide reaction of aldehydes and ketones reaction of amide with naoh reaction of amine group with water reaction of amine with hydroxyl reaction of amines with nitrous acid mechanism reaction of an amine with water is best represented by reaction of aniline with chlorosulfonic acid

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