Downloads
Abstract
ZnCl2 in 1-allyl-3-methylimidazolium trifloromethanesulfonate was found to be a good catalyst for the Friedel-Crafts acylation. The ketone product was isolated easily from the reaction mixture. The reactions were found to proceed smoothly under microwave irradiation. The isolated yield was high with 95% selectivity of pisomer within a few minutes. Moreover, ZnCl2 and ion liquid have been recovered and reused several times without significant loss of catalytic activity.
Issue: Vol 2 No 1 (2018)
Page No.: 34-39
Published: Jan 6, 2019
Section: Original Research
DOI: https://doi.org/10.32508/stdjns.v2i1.671
Download PDF = 689 times
Total = 689 times
Most read articles by the same author(s)
- Nguyen Thi Xuan Trang, Tran Hoang Phuong, The alkylation of indole with benzaldehyde derivatives catalyzed by 1-(4- sulfobutyl)-3-methylimidazolium hydrogene sulfate ion gel , Science & Technology Development Journal: Natural Sciences: Vol 2 No 1 (2018)
- Nguyen Truong Hai, Tran Hoang Phuong, A green method for the acylation of secondary alcohols with [CholineCl][ZnCl2]3-catalyzed by ultrasonic method , Science & Technology Development Journal: Natural Sciences: Vol 1 No 6 (2017)