acetic anhydride reaction with secondary amine


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  • What are symmetrical and unsymmetrical acid anhydrides?

    Both symmetrical and unsymmetrical acid anhydrides can be prepared in this way. The chemistry of acid anhydrides is similar to that of acid chlorides, although anhydrides react more slowly. Thus, acid anhydrides react with water to form acids, with alcohols to form esters, with amines to form amides, and with LiAlH 4 to form primary alcohols.

  • Can acyl chloride acylate a tertiary amine?

    Acyl chlorides and acid anhydrides react with primary and secondary amines without the presence of heat to form amides. Tertiary amines cannot be acylated due to the absence of a replaceable hydrogen atom. With the much less active benzoyl chloride, acylation can still be performed by the use of excess aqueous base to facilitate the reaction.

  • Can amines react with acetic anhydride?

    Amines were allowed to react with AFA, which was generated in situ from excess formic acid and acetic anhydride at −20 °C ( Scheme 4 ). The reaction reached completion for most amines in less than 15 min and the resulting formamides were isolated in yields of 97%–100%.

Reaction of Amines with Acetic Anhydride

Reaction of Amines with Acetic Anhydride

Imine and Enamine Formation Reactions With Reductive Amination

Imine and Enamine Formation Reactions With Reductive Amination

Amine Synthesis Reactions

Amine Synthesis Reactions

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