What is Hinsberg’s reagent?
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Hinsberg’s reagent is a chemical reagent used in organic chemistry to distinguish between primary, secondary, and tertiary amines. It is named after the German chemist Oscar Hinsberg, who developed it.
Hinsberg’s reagent is composed of benzene sulfonyl chloride (C₆H₅SO₂Cl), also known as benzenesulfonyl chloride or simply benzoyl chloride. The chemical structure of benzene sulfonyl chloride is C₆H₅SO₂Cl.
When Hinsberg’s reagent reacts with an amine, it forms a sulfonamide derivative. The reaction proceeds differently depending on the nature of the amine:
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Primary amines react with Hinsberg’s reagent to form N-alkylbenzenesulfonamides.
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Secondary amines react with Hinsberg’s reagent to form N,N-dialkylbenzenesulfonamides.
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Tertiary amines do not react with Hinsberg’s reagent under normal conditions.