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DBN‐Catalyzed Regioselective Acylation of Carbohydrates and Diols in Ethyl Acetate
Author(s) -
Ren Bo,
Zhang Mengyao,
Xu Shijie,
Gan Lu,
Zhang Li,
Tang Lin
Publication year - 2019
Publication title -
european journal of organic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.825
H-Index - 155
eISSN - 1099-0690
pISSN - 1434-193X
DOI - 10.1002/ejoc.201900776
Subject(s) - acylation , chemistry , regioselectivity , catalysis , organic chemistry , ethyl acetate
The 1,5‐diazabicyclo[4.3.0]non‐5‐ene (DBN)‐catalyzed regioselective acylation of carbohydrates and diols in ethyl acetate has been developed. The hydroxyl groups can be selectively acylated by the corresponding anhydride in EtOAc in the presence of a catalytic amount (as low as 0.1 equiv.) of DBN at room temperature to 40 °C. This method avoids metal catalysts and toxic solvents, which makes it comparatively green and mild, and it uses less organic base compared with other selective acylation methods. Mechanism studies indicated that DBN could catalyze the selective acylation of hydroxyl moieties through a dual H‐bonding interaction.