R-（＋）-α-硫辛酸的合成工艺.pdfVIP

学兔兔 化 工 进 展 2012年第31卷第6期 CHEMICAL INDUSTRYAND ENGINEERING PROGRESS ·1325· (+)． 硫辛酸的合成工艺 冷一欣，牛锦森，黄春香 (常州大学石油化工学院，江苏 常州I 213164) 摘 要：以 6,8．二氯辛酸为原料， (一)一n一苯乙胺为拆分剂进行拆分反应得到 R．(+)一6，8．二氯辛酸；经酯化制得 ． (+)一6，8．二氯辛酸乙酯；后经硫化水解一步合成 ．(+) 一硫辛酸。考察了投料比、溶剂、催化剂、温度等条件对 产物收率、比旋光度的影响。结果表明：拆分反应较佳条件为n[S-(一)一d一苯乙胺]：n(6,8-二氯辛酸)=0．45：1， 溶剂为乙酸乙酯；酯化反应较佳条件为催化剂为对甲苯磺酸，反应时间7h；硫化反应较佳条件为温度为65℃； 相转移催化剂用量0．4 g，总收率为44．3％。通过红外光谱、比旋光度、核磁共振等对产物和中间产物进行了表 征。 关键词：6,8一二氯辛酸；拆分；酯化；硫化；R一(+)一 ．硫辛酸 中图分类号：o 626．2 文献标志码：A 文章编号：1000—6613(2012)06—1325—05 Synthesis of厣(+)一a-lipoic acid LENG Hxin，NIUJinsen，HUANG Chunxiang (School ofPetrochemical Engineering，Changzhou University，Changzhou 213 164，Jiangsu，China) Abstract：R．(+)．6，8一dichlorooctanic acid was obtained in chiral resolution of 6，8．dich1orooctanic acid by using chiral split agent s-(-)一 —phenylethylamine．R一(+)一 一lipoic acid was synthesized by sulfuration and hydrolysis from R一(+)一6，8一dichloro0ctanic acid ethyl ester that was prepared through esterfication reaction．The conditions were investigated and the results showed that the yield and specific rotation were influenced by feed ratio，solvent，catalyst and reaction temperature．Proper experimental condition for chiral reaction was found as：n[S-(-)一。【-phenylethylamine]： (6，8-dichlorooctanic acid)：0．45：1， solvent was ethyl acetate．The optimal esterfication reaction conditions was found as：the catalyst was P—toluene sulfonic acid，reaction time 7 h．The optimum conditions of sulfuration reaction were found as：reaction t