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对甲苯磺酰氯合成研究

Study on the Synthesis of p-Toluenesulfonyl Chloride

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【作者】 陈钟秀蒋林峰丁同富徐芸孙镭俞兴源

【Author】 CHEN Zhong-xiu1, JIANG Lin-feng1, DING Tong-fu1, XU Yun2, SUN Lei2, YU Xing-yuan2 (1. College of Materials and Chemical Engineering, Zhejiang University, Hangzhou 310027, China; 2. Jiahua Chemicals Corporation, Jiaxing 314021, China)

【机构】 浙江大学材化学院浙江嘉化实业股份有限公司浙江嘉化实业股份有限公司 浙江杭州310027浙江杭州浙江嘉兴314021314021

【摘要】 以甲苯、氯磺酸、三氯氧磷为原料,氯化铵为催化剂合成对甲苯磺酰氯。研究了氯磺酸、三氯氧磷、催化剂用量及反应时间对氯磺化反应的影响。得出了最佳原料摩尔比:甲苯:氯磺酸:三氯氧磷:氯化铵为1:1.3:0.6:0.1,其产品收率达98.85%,纯收率为97.86%(对甲苯磺酰氯85.41%,邻甲苯磺酰氯12.45%);同时酸性废水比原工艺减少了70%以上。

【Abstract】 Taking toluene, chlorosulfonic acid and phosphoryl chloride as raw materials, p-toluenesulfonyl was synthesized. The effects of amount of chlorosulfonic acid, phosphoryl chloride, and reaction temperature on the yield of p-toluenesulfonyl chloride were investigated. The optimal reaction condition was obtained by the catalyst selection experiments and the orthogonal test. The ammonium chloride was chosen as the suitable catalyst and the optimum molar ratio of toluene, chlorosulfonic acid, phosphoryl chloride and ammonium chloride was found to be 1,1.3,0.6 and 0.1. Under the optimal reaction condition, the yield and pure yield of toluenesulfonyl chloride are up to 98.85% and 97.86% respectively. The yield of p-toluenesulfonyl chloride and o-toluenesulfonyl chloride achieve 85.41% and 12.45% respectively. Acidic waste fluid is dropped off 70% or more. The process is successful for reducing the cost and the environmental protection.

【基金】 浙江省嘉兴市政府资助项目。
  • 【文献出处】 高校化学工程学报 ,Journal of Chemical Engineering of Chinese Universities , 编辑部邮箱 ,2004年02期
  • 【分类号】TQ247
  • 【被引频次】12
  • 【下载频次】1424
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