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A Direct, Early Stage Guanidinylation Protocol for the Synthesis of Complex Aminoguanidine-containing Natural Products
Published on: September 9, 2016
Selective and Waste-Free Isolation of High Purity Primary Amines from Amine and Reaction Mixtures by Selective
Bernd Rienhoff1, Dilara Mede1, Mara Schöler1
1Department for Biochemical and Chemical Engineering, Laboratory of Industrial Chemistry, TU Dortmund University, Emil-Figge-Straße 66, Dortmund, 44227, Germany.
None:
The isolation of primary amines from secondary and tertiary amines presents a significant challenge in their sustainable production, and existing strategies are either multistep, energy-demanding, or waste-intensive. We present an efficient process that utilizes the distinct solubility profiles of ammonium carbamate species formed through waste-free and reversible salt formation of primary amines and CO2. This selective ammonium carbamate crystallization (SACC) enables the purification of challenging amine mixtures. Starting from 35% initial primary amine purity, SACC achieves very high isolated yields of up to 94% and excellent purities exceeding 99%. Additionally, the separation of secondary from tertiary amines with 86% yield and 91% purity and the fractional crystallization of primary, secondary, and tertiary amines with yields ranging from 83% to 94% and purities from 90% to > 99% were successfully achieved. SACC was also successfully employed in the alcohol amination with ammonia/ammonia alkylation to isolate primary amines with high yields of up to 84% and excellent purities exceeding 99% using a homogeneous Ru/xantphos catalyst system. The observed average metal and phosphorus losses were at a minimal level of < 1 wt% of the initial amounts. Based on this high catalyst retention, the additional potential of SACC for recycling the homogeneous catalyst was demonstrated.
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