Conversion of N-Acetylglucosamine to 3-Acetamido-5-Acetylfuran over Al-Exchanged Montmorillonite.
Kiyoyuki YamazakiNorihito HiyoshiAritomo YamaguchiPublished in: ChemistryOpen (2023)
3-Acetamido-5-acetylfuran (3A5AF) is a potential platform compound for the production of nitrogen-containing pharmaceuticals and chemicals. 3A5AF can be obtained by dehydration of chitin or its monomer, N-acetylglucosamine (NAG). Here, we examined the use of solid catalysts for the dehydration of NAG to 3A5AF to achieve a more economical process that uses a recyclable catalyst. NAG was dehydrated using various solid catalysts in the presence of NaCl and N,N-dimethyl acetamide as solvent at 433 K. The yield of 3A5AF with the solid catalysts decreased in the following order: Al-exchanged montmorillonite>H-ZSM-5 (SiO 2 /Al 2 O 3 =40)>H-montmorillonite (K-10)>Amberlyst15>H-ZSM-5 (SiO 2 /Al 2 O 3 =300)>TiO 2 >γ-Al 2 O 3 >ZrO 2 >SiO 2 ⋅ MgO>Na-montmorillonite. The highest yield of 3A5AF (14 %) was obtained with the Al-exchanged montmorillonite. The montmorillonite catalysts were characterized by using inductively coupled plasma optical emission spectroscopy, energy-dispersive X-ray spectroscopy, N 2 adsorption, Fourier-transformed infrared spectroscopy, X-ray diffraction, and 27 Al magic-angle spinning nuclear magnetic resonance spectroscopy (MAS-NMR). In addition, a combined catalyst of Al-exchanged montmorillonite and Cl - from synthetic hydrotalcite was found to be an active and recyclable solid catalyst for NAG dehydration to 3A5AF.
Keyphrases
- high resolution
- highly efficient
- atrial fibrillation
- ionic liquid
- solid state
- metal organic framework
- magnetic resonance
- room temperature
- computed tomography
- mass spectrometry
- risk assessment
- high speed
- quantum dots
- carbon dioxide
- gas chromatography mass spectrometry
- transition metal
- ms ms
- amino acid
- tandem mass spectrometry
- electron microscopy