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亚糠基丙酮的合成工艺研究
引用本文:刘洋,李帅,廖蓉苏,陈红艳.亚糠基丙酮的合成工艺研究[J].精细化工中间体,2008,38(4).
作者姓名:刘洋  李帅  廖蓉苏  陈红艳
作者单位:北京林业大学,材料科学与技术学院,北京,100083
摘    要:在稀碱条件下,由糠醛和丙酮经羟醛缩合反应可制备亚糠基丙酮。通过对影响亚糠基丙酮质量和收率的主要因素原料配比、反应温度、碱浓度、反应时间等单因素实验,探索出合成亚糠基丙酮的优化反应条件为:原料配比n(糠醛)∶n(丙酮)=1.0∶1.0、反应温度40℃、氢氧化钠溶液浓度为0.10mol/L、反应时间5h。产品收率30.2%,纯度达98%以上,并用红外光谱和气相色谱-质谱对产品进行了表征。

关 键 词:亚糠基丙酮  羟醛缩合  糠醛  丙酮

Synthesis Technology of 4-(2-Furyl)3-buten-2-one
LIU Yang,LI Shuai,LIAO Rong-su,CHEN Hong-yan.Synthesis Technology of 4-(2-Furyl)3-buten-2-one[J].Fine Chemical Intermediates,2008,38(4).
Authors:LIU Yang  LI Shuai  LIAO Rong-su  CHEN Hong-yan
Abstract:In alkaline condition,the aldolic condensation reaction of furfural on acetone gives the 4-(2-furyl)3-buten-2-one. The factors which mostly affect the quality and output of the product including molar proportion of reagents,reaction temperature,alkaline concentration and reaction time are analyzed. After orthogonal experiment,it is concluded that the optimized reaction condition is that acetone and furfural are charged with equal molar quantities at 40℃ with sodium hydroxide(0.10 mol/L)and the operation time 5 h. In addition,IR and GC/MS are used to confirm the product.
Keywords:4-(2-furyl)3-buten-2-one  aldolic condensation  furfural  acetone
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