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5-Amino-1-pentanol

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Through Amine, Alkane and Ammonia

Occurrence and preparation

The complete hydrogenation of furfural (furan-2-aldehyde) yields tetrahydrofurfuryl alcohol (2-hydroxymethyltetrahydrofuran), which undergoes ring expansion upon dehydration to give dihydropyran. Dihydropyran reacts with ammonia in a reductive amination under ring opening to produce 5-amino-1-pentanol.

Product yields of up to 85% can be achieved with a continuous process using a nickel-hydrotalcite catalyst.

Similarly, the hemiacetal 2-hydroxytetrahydropyran that is formed from dihydropyran with hydrochloric acid can be converted to 5-amino-1-pentanol by reductive amidation with ammonia and hydrogen upon water elimination.

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