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一种2‑(1‑羟基‑4‑酮‑2,5‑环己二烯)‑吡喃‑4‑酮的合成方法

申请公布号:CN106083790A

申请号:CN201610416229.2

申请日期:2016.06.14

申请公布日期:2016.11.09

申请人:
武昌理工学院

发明人:王小华;阮金兰;刘阳

分类号:C07D309/38(2006.01)I

主分类号:C07D309/38(2006.01)I

代理机构:
武汉宇晨专利事务所 42001

代理人:王敏锋

地址:430223 湖北省武汉市江夏大道16号

摘要:本发明公开了一种2‑(1‑羟基‑4‑酮‑2,5‑环己二烯)‑吡喃‑4‑酮的合成方法,其步骤是:1)在氮气保护和碱存在的条件下,室温下对甲氧基苯乙酮进行硅醚保护,得到1‑(4‑甲氧基苯基)‑1‑三甲基硅氧乙烯;2)在氮气保护和弱酸性条件下,1‑(4‑甲氧基苯基)‑1‑三甲基硅氧乙烯和草酰氯在0‑5℃下发生缩合反应,得到5‑(4‑甲氧基苯基)‑2,3–二氢呋喃–2,3–二酮;3)5‑(4‑甲氧基苯基)‑2,3–二氢呋喃–2,3–二酮与乙烯基乙醚在回流的条件得到2‑(4‑甲氧基苯基)‑4H‑吡喃‑4‑酮;4)氮气保护下,2‑(4‑甲氧基苯基)‑4H‑吡喃‑4‑酮脱去甲基得到2‑(4‑羟基苯基)‑4H‑吡喃‑4‑酮;5)室温下,2‑(4‑羟基苯基)‑4H‑吡喃‑4‑酮在氧化剂的作用下发生反应得到2‑(1‑羟基‑4‑酮‑2,5‑环己二烯)‑吡喃‑4‑酮。该方法操作简单,原料便宜易得,收率高。

主权项:一种2‑(1‑羟基‑4‑酮‑2,5‑环己二烯)‑吡喃‑4‑酮的合成方法,其特征在于包括如下步骤:1)在氮气保护和碱存在的条件下,室温下对甲氧基苯乙酮进行硅醚保护,得到1‑(4‑甲氧基苯基)‑1‑三甲基硅氧乙烯,反应式如下:<img file="FDA0001016646540000011.GIF" wi="911" he="343" />2)在氮气保护和弱酸性条件下,1‑(4‑甲氧基苯基)‑1‑三甲基硅氧乙烯和草酰氯在0‑5℃下发生缩合反应,得到5‑(4‑甲氧基苯基)‑2,3–二氢呋喃–2,3–二酮,反应式如下:<img file="FDA0001016646540000012.GIF" wi="1294" he="447" />3)5‑(4‑甲氧基苯基)‑2,3–二氢呋喃–2,3–二酮与乙烯基乙醚在回流的条件得到2‑(4‑甲氧基苯基)‑4H‑吡喃‑4‑酮,反应式如下:<img file="FDA0001016646540000013.GIF" wi="1246" he="448" />4)氮气保护下,2‑(4‑甲氧基苯基)‑4H‑吡喃‑4‑酮脱去甲基得到2‑(4‑羟基苯基)‑4H‑吡喃‑4‑酮,反应式如下:<img file="FDA0001016646540000021.GIF" wi="837" he="431" />5)室温下,2‑(4‑羟基苯基)‑4H‑吡喃‑4‑酮在氧化剂的作用下发生反应得到2‑(1‑羟基‑4‑酮‑2,5‑环己二烯)‑吡喃‑4‑酮,反应式如下:<img file="FDA0001016646540000022.GIF" wi="846" he="413" />

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