REACTION OF SOME SALICYL ALDEHYDE DERIVATIVES WITH AMINES ANDPHENYL ACETYLENE

DOI: 10.18173/2354-1059.2020-0048

  • Nguyen Thi Minh Trang
  • Tran Thi Thu Trang
  • Duong Quoc Hoan
Từ khóa: propargylamine, multicomponent reaction, aldehyde-alkyne-amine, solvent-free, metal-free.

Tóm tắt

Salicylic aldehydes, amine, and phenyl acetylene could react under the solvent-free, metal-free conditions to form propargylamines 1-4 via A3 coupling reaction. The yield of the reaction was up to 83% for 5h. In acetonitrile, the amine became a catalyst to form 6-bromo-3-(5-bromo-2-hydroxybenzyl)-2-phenyl-4Hchromen-4-one (5). Under microwave conditions, it took about 20 min to complete the reaction and gave the same yields as theconventional method. Structures of these compounds were firm with NMR, MS spectra. 

điểm /   đánh giá
Phát hành ngày
2021-05-10
Chuyên mục
BAI BÁO