4-(1-tert-butoxy-2-methyl-1-oxopropan-2-ylthio)benzoic acid 、
1-(4-methylbenzyl)-4-(hydroxymethyl)-1H-1,2,3-triazole 、
N,N'-二环己基碳二亚胺 在
4-二甲氨基吡啶 N,N-二环己脲 、
ethyl acetate n-hexane 作用下,
以
二氯甲烷 为溶剂,
反应 16.0h,
以to give (1-(4-methylbenzyl)-1H-1,2,3-triazol-4-yl)methyl 4-(1-tert-butoxy-2-methyl-1-oxopropan-2-ylthio)benzoate as a white solid (0.62 g), 1H NMR (400 MHz, DMSO-d6) δ 8.27 (s, 1H); 7.91 (d, J=8.4 Hz, 2H); 7.55 (d, J=8.4 Hz, 2H); 7.20 (dd, J=8.0 and 24.4 Hz, 4H); 5.55 (s, 2H); 5.38 (s, 2H); 2.27 (s, 3H); 1.42 (s, 6H); 1.33 (s, 9H)的产率得到(1-(4-methylbenzyl)-1H-1,2,3-triazol-4-yl)methyl 4-(1-tert-butoxy-2-methyl-1-oxopropan-2-ylthio)benzoate