TY - JOUR
T1 - Amino acid based natural deep eutectic solvents
T2 - An efficient catalyst and solvent for N-acetyl-D-glucosamine conversion into organonitrogen chemicals
AU - Zhao, Jiancheng
AU - Guo, Zhaohui
AU - Marcus Pedersen, Christian
AU - Jia, Lingyu
AU - Jia, Shiyu
AU - Hou, Xianglin
AU - Wang, Yingxiong
AU - Qiao, Yan
N1 - Funding Information:
The authors thank for National Natural Science Foundation of China ( 22075308 ) and Natural Science Foundation of Shanxi Province ( 202103021224439 ) for financial support. Lingyu Jia acknowledges supporting of Natural Science Foundation of Henan Province ( 242300421601 ).
Publisher Copyright:
© 2024 Elsevier B.V.
PY - 2024
Y1 - 2024
N2 - Organonitrogen chemicals are widely used and in great demand in the food, pharmaceutical and chemical industries. Hence, it is important to develop green and efficient synthesis paths to organonitrogen chemicals for their use as new resources. Herein, we propose the preparation of organonitrogen chemicals from chitin biomass monomer N-acetyl-D-glucosamine (GlcNAc) promoted by natural deep eutectic solvents (NADESs). The selective generation of 3-acetamido-5-(1′,2′-dihydroxyethyl) furan (Chromogen III) and 3-acetamido-5-acetylfuran (3A5AF) from GlcNAc was achieved by the design of NADESs components. GlcNAc reacts in binary NADES proline-glycerol (Pro-Gly) to generate 26 % of Chromogen III and 39 % of 3A5AF in ternary NADES proline-glycerol-lactic acid (Pro-Gly-LA). In addition, the intermolecular hydrogen bonds in NADESs were confirmed through 1H diffusion-ordered spectroscopy (DOSY) NMR technology. And the results of 13C NMR chemical shift titration indicated interaction between NADESs and the C3 and C6 position of GlcNAc. Based on the NMR experiments a mechanism is proposed.
AB - Organonitrogen chemicals are widely used and in great demand in the food, pharmaceutical and chemical industries. Hence, it is important to develop green and efficient synthesis paths to organonitrogen chemicals for their use as new resources. Herein, we propose the preparation of organonitrogen chemicals from chitin biomass monomer N-acetyl-D-glucosamine (GlcNAc) promoted by natural deep eutectic solvents (NADESs). The selective generation of 3-acetamido-5-(1′,2′-dihydroxyethyl) furan (Chromogen III) and 3-acetamido-5-acetylfuran (3A5AF) from GlcNAc was achieved by the design of NADESs components. GlcNAc reacts in binary NADES proline-glycerol (Pro-Gly) to generate 26 % of Chromogen III and 39 % of 3A5AF in ternary NADES proline-glycerol-lactic acid (Pro-Gly-LA). In addition, the intermolecular hydrogen bonds in NADESs were confirmed through 1H diffusion-ordered spectroscopy (DOSY) NMR technology. And the results of 13C NMR chemical shift titration indicated interaction between NADESs and the C3 and C6 position of GlcNAc. Based on the NMR experiments a mechanism is proposed.
KW - 3A5AF
KW - Chromogen III
KW - N-acetyl-D-glucosamine
KW - Natural deep eutectic solvents
KW - NMR
U2 - 10.1016/j.molliq.2024.126006
DO - 10.1016/j.molliq.2024.126006
M3 - Journal article
AN - SCOPUS:85204220231
SN - 0167-7322
VL - 413
JO - Journal of Molecular Liquids
JF - Journal of Molecular Liquids
M1 - 126006
ER -