Two novel reactive monomers 2,4 bis(2 allyl phenoxy) 6 N,N dialkylamino 1,3,5 triazine (alkyl=methyl, ethyl) were synthesized in one pot reaction of cyanuric chloride, 2 allyl phenol with dialkylamine in acetone/water...Two novel reactive monomers 2,4 bis(2 allyl phenoxy) 6 N,N dialkylamino 1,3,5 triazine (alkyl=methyl, ethyl) were synthesized in one pot reaction of cyanuric chloride, 2 allyl phenol with dialkylamine in acetone/water in the presence of aq. NaOH. The products have been characterized by FTIR, 1H NMR, 13 C NMR and elemental analysis.展开更多
Solanesyl bromide(Ⅱ) was reacted with diethanolamine to give solanesyl diethanolamine(Ⅲ) which was acylated with 3,4,5 trimethoxybenzoyl chloride, acetic anhydride, benzoyl chloride and cinnamyl chloride to give N,N...Solanesyl bromide(Ⅱ) was reacted with diethanolamine to give solanesyl diethanolamine(Ⅲ) which was acylated with 3,4,5 trimethoxybenzoyl chloride, acetic anhydride, benzoyl chloride and cinnamyl chloride to give N,N di[(3,4,5 trimethoxybenzoyloxy)ethyl]solanesylamine(Ⅳ), N,N di[(acetyloxy)ethyl] solanesylamine(Ⅴ), N,N di[(benzoyloxy)ethyl]solanesylamine(Ⅵ), N,N di[(cinnyloxy)ethyl]solanesylamine(Ⅶ) respectively. The structures of compounds Ⅲ～Ⅶ were confirmed by IR, 1H NMR, MS and elemental analysis.展开更多
文摘Two novel reactive monomers 2,4 bis(2 allyl phenoxy) 6 N,N dialkylamino 1,3,5 triazine (alkyl=methyl, ethyl) were synthesized in one pot reaction of cyanuric chloride, 2 allyl phenol with dialkylamine in acetone/water in the presence of aq. NaOH. The products have been characterized by FTIR, 1H NMR, 13 C NMR and elemental analysis.
文摘Solanesyl bromide(Ⅱ) was reacted with diethanolamine to give solanesyl diethanolamine(Ⅲ) which was acylated with 3,4,5 trimethoxybenzoyl chloride, acetic anhydride, benzoyl chloride and cinnamyl chloride to give N,N di[(3,4,5 trimethoxybenzoyloxy)ethyl]solanesylamine(Ⅳ), N,N di[(acetyloxy)ethyl] solanesylamine(Ⅴ), N,N di[(benzoyloxy)ethyl]solanesylamine(Ⅵ), N,N di[(cinnyloxy)ethyl]solanesylamine(Ⅶ) respectively. The structures of compounds Ⅲ～Ⅶ were confirmed by IR, 1H NMR, MS and elemental analysis.
