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Kyodai硝化法合成1-硝基金刚烷
引用本文:张琳,马伟,罗军.Kyodai硝化法合成1-硝基金刚烷[J].精细化工中间体,2009,39(6):22-24,39.
作者姓名:张琳  马伟  罗军
作者单位:南京理工大学化工学院,江苏,南京,210094
摘    要:将二氧化氮-臭氧体系用于金刚烷的直接硝化合成重要中间体1-硝基金刚烷,研究二氧化氮用量、反应时间、反应温度和臭氧流量等因素对反应的影响,在n(金刚烷):n(二氧化氮)=1:15、臭氧流量为0.4L/min、-30℃下反应2h的优化条件下,金刚烷的转化率为99.9%,1-硝基金刚烷的收率为90.9%,当n(金刚烷):n(二氧化氮)=1:30时,1-硝基金刚烷的收率可达92.1%。

关 键 词:1-硝基金刚烷  金刚烷  Kyodai硝化  绿色化学工艺

Synthesis of 1-Nitroadamantane via Kyodai Nitration
ZHANG Lin,MA Wei,LUO Jun.Synthesis of 1-Nitroadamantane via Kyodai Nitration[J].Fine Chemical Intermediates,2009,39(6):22-24,39.
Authors:ZHANG Lin  MA Wei  LUO Jun
Affiliation:(School of Chemical Engineering, Nanjing University of Science and Technology, Nanjing 21009, China)
Abstract:1 -Nitroadamantane was synthesized from adamantine by direct nitration with NO2-O3. The reaction afforded 1-nitroadamantane in 90.9% yield with adamantine conversion of 99.9% under the optimized conditions: n (adamantine) ∶ n (NO2) = 1 ∶ 15, flow rate of O3 = 0.4 L / min, reaction temperature -30℃, reaction time 2 h. Moreover, when 30 equivalents of NO2 was used, 1-nitroadamtane was obtained in a higher yield of 92.1%. This technology avoids use of nitrous acid, and therefore is a green process.
Keywords:1-nitroadamantane  adamantine  Kyodai nitration  green chemical process
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