Question

Why gabriel phthalimide reaction is preferred for primary amine synthesis?

Answer 1

$\huge\star\underline\mathcal\orange{ANSWER}$

Gabriel Phthalimide synthesis is preferred for the syntheaizing amines. Gabriel Phthalimide synthesis results in the formation of primary amine only.

Answer 2

Explanation:

Gabriel phthalimide synthesis is a very convenient method for the preparation of pure aliphatic amines ( especially primary amines) Phthalimide on treatment with ethanolic KOH gives potassium phthalimide which on heating with a suitable alkyl hallide gives N-substituted phthalimides. These upon susbsequent hydrolysis with dil.HCl under pressure or with alkali gives primary amines.

Step 1: Phthalimide is treated with KOH to form potassium phthalimide

Step 2: Potassium phthalimde is treated with suitable alkyl hallide to form N-substituted phthalimides.

Step 3: N-substituted phthalimides undergoes hydrolysis in the prsence of dil HCl or with alkali(NaOH) to give primary amines.

Overall reaction:

∴ Gabriel phthalimide synthesis results in the formation of primary(1° amine) only. Secondary or tertiary amines are not formed through this synthesis. Hence, Gabriel phthalimide synthesis preferred for the formation of primary amines only.