50 6 |  | Vol. 50 No. 6 | 2020 12 | Dec 2020 |
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ٙĿtˎgw
25-cϩxԆκpMBH |
_ gꐘŝ*
ƼW(xu) W(xu)W(xu)Ժ ϲ 330013 |
ժҪԿYԴԭøЧԭӽ(jng)ԵķOӋϳµĹܷԹǞԭһϳ25-ૣDFF 41%DFF ͱϩԭM(jn)Morita-Baylis-HillmannMBHڲͬ܄lxԺϳɆμpӳɮa(chn)1 2Զh(hun)-ˮVV=11܄ͬr(sh)@Æμpl(f)MBH Įa(chn)1 2ʷքe 46% 37%Լ״܄txԫ@Æμl(f)MBH Įa(chn)1 32%a(chn)1H NMRM(jn)˽Y_C |
P(gun)I~ܱϩMBH 25-ૣDFFx |
ЈD(li)̖O629.1īIRaA¾̖1009-9212202006-0037-04 |
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Selective Mono- and Bis-MBH Reaction Between 2,5-Diformyl Furan and Methyl Acrylate |
WANG Li-juan, HE Xian-qin, LUO Huan, DING Yu-hao, CHEN Rong-jian, CHENG Chuan-jie*
(School of Chemistry and Chemical Engineering, Jiangxi Science&Technology Normal University, Nanchang 330013, China) |
AbstractIt is of great significance to synthesize functional molecules via highly efficient and atom-economic reactions by using renewable resource materials. Herein, firstly, 2,5-diformyl furan (DFF) was synthesized from fructose in one step with a yield of 41%. Then, MBH reactions were conducted between DFF and methyl acrylate,and selective products in different solvents were obtained. When 1,4-dioxane/water (VV=11) was utilized, both mono-acrylate and di-acrylate products were obtained at yield of 46% and 37%, respectively; while the sole methanol solvent gave only mono-acrylate with a yield of 32%. All the products were characterized by 1H NMR. The synthesized functional acrylates may further undergo reactions to prepare more valuable small molecules as well as polymers. |
Key wordsfunctional acrylates; MBH reaction; 2,5-diformyl furan (DFF); selectivity |
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ĿȻƌW(xu)Ŀ (21564004)ƼW(xu)(chung )¿Ŀ
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ߺ(jin)飺 (1998)ŮɹźͺҪЙCܷOӋϳɷоE-mail: 2569974376@qq.com
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(lin) ϵ ˣ̂ʿҪÿYԴOӋϳЙCܷӷоE-mail: chengcj530@163.com
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ոڣ2020-10-14
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