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第 35 卷第 5 期Vol. 35 No. 5
2005 年 10 月Oct 2005

所屬欄目:有機合成原料

原位氧化氯化合成3-氯丁酮
鐘文周; 尹篤林; 徐瓊; 王季惠; 唐迪(湖南師范大學(xué)精細催化合成研究所教育部化學(xué)生物學(xué)及中藥分析重點(diǎn)實(shí)驗室; 湖南長(cháng)沙)
摘 要:利用鹽酸-過(guò)氧化氫作反應物,通過(guò)原位氯化反應合成3-氯丁酮?疾炝嗽吓 比、反應時(shí)間、反應溫度、及金屬鹽的加入對反應結果的影響。以CuCl2作催化劑,丁酮、鹽酸、過(guò)氧 化氫的摩爾配比為2∶1∶1.3時(shí),回流溫度下反應5h,丁酮轉化率為52.43%,3-氯丁酮選擇性 達76%,分餾得到的產(chǎn)品的純度98%以上。
關(guān)鍵詞:氧化氯化; 鹽酸-過(guò)氧化氫; 3-氯丁酮
中圖分類(lèi)號:TQ224.5  文獻標識碼:A  文章編號:1009-9212(2005)05-0032-03
Synthesis of 3-chloro-2-butanone by oxidation-chlorination in situ
ZHONG Wen-zhou; YIN Du-lin; XU Qiong; WANG Ji-hui; TANG Di Institute of Fine Catalysis and Synthesis; Key Laboratory of Chemical Biology & Traditional Chinese Medicine Research; Hunan Normal University; Changsha 410081; China
Abstract:3-chloro-2-butanone was synthesized by chlorination in situ with HC1-H2O2. The influences of reaction conditions such as mole ratio, reaction time, reaction temperature and some metal salts were examined in detail. The optimum preparation conditions were CuCl2 as catalyst, n(butanone):n(HCl):n(H2O2)=2:l:1.3, reaction temperature 78℃ and reaction time is 5h. the conversion of butanone amount to 52.43%, the selectivity of 3-chloro-2-butanone is over 76% and its purity is over 98%.
Key words:oxidation-chlorination; HCl-H2O2; 3-chloro-2-butanone
收稿日期:2005-06-30
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