TY - JOUR
T1 - Ultrasound accelerated sulfonylation of amines by p-acetamidobenzenesulfonyl chloride using Mg–Al hydrotalcite as an efficient green base catalyst
AU - Truong, Binh Nhat
AU - Le, Luong Huu
AU - Chau, Duy-Khiem Nguyen
AU - Duus, Fritz
AU - Luu, Thi Xuan Thi
PY - 2016
Y1 - 2016
N2 - The sulfonylation reaction of various aliphatic, alicyclic, aromatic, and hetero-aromatic amines with p-acetamidobenzenesulfonyl chloride has been investigated using different types of base catalysis under varied reaction conditions. Mg–Al hydrotalcite, characterizable as an inexpensive, reusable, and green solid catalyst, was found to be the most efficient catalyst, when the reaction is carried out in a minimum volume of solvent (acetone). The reaction was found to be accelerated drastically with the support of ultrasound irradiation, affording the sulfonamides in yields better or equivalent to those obtained under the longer lasting conventional stirring conditions.
AB - The sulfonylation reaction of various aliphatic, alicyclic, aromatic, and hetero-aromatic amines with p-acetamidobenzenesulfonyl chloride has been investigated using different types of base catalysis under varied reaction conditions. Mg–Al hydrotalcite, characterizable as an inexpensive, reusable, and green solid catalyst, was found to be the most efficient catalyst, when the reaction is carried out in a minimum volume of solvent (acetone). The reaction was found to be accelerated drastically with the support of ultrasound irradiation, affording the sulfonamides in yields better or equivalent to those obtained under the longer lasting conventional stirring conditions.
KW - Mg–Al hydrotalcite
KW - sulfonamide synthesis
KW - disulfonylation of amine
KW - desulfonylation
KW - ultrasound irradiation
U2 - 10.1080/17415993.2016.1193180
DO - 10.1080/17415993.2016.1193180
M3 - Journal article
VL - 37
SP - 515
EP - 528
JO - Journal of Sulfur Chemistry
JF - Journal of Sulfur Chemistry
SN - 1741-5993
IS - 5
ER -