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DOI: 10.1055/s-0031-1289890
Hexamethylenetetramine
Publikationsverlauf
Publikationsdatum:
11. November 2011 (online)

Introduction
Hexamethylenetetramine (HMTA) is a heterocyclic organic compound having a symmetric tetrahedral cage-like structure, whose four ‘corners’ are nitrogen atoms and ‘edges’ are methylene groups. It is also known as hexamine. It behaves like an amine base and known for its versatile role in organic chemistry. It plays an important role in formylation (Duff reaction), [¹] [²] conversion of benzyl halides into corresponding aldehydes (Sommelet reaction), [³] and synthesis of amines (Delépine reaction). [4]
HMTA is a useful reagent in the conversion of ethyl 2-(4-hydroxyphenyl)-4-methylthiazole-5-carboxylate into ethyl 2-(3-formyl-4-hydroxyphenyl)-4-methylthiazole-5-carboxylate, an important step in the synthesis of febuxostat (hypouricemic agent). [5] Apart from these applications, hexamethylenetetramine is also known for the synthesis of explosives like RDX (hexogen). [6] Further, it has wide applications in polymer chemistry. [7] HMTA is commercially available and first synthesized by Butlerov via reaction of formaldehyde with ammonia. [8]
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