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α-三氟甲基乙胺合成工艺研究
引用本文:徐光辉,朱国彪. α-三氟甲基乙胺合成工艺研究[J]. 广东化工, 2012, 39(1): 194-195
作者姓名:徐光辉  朱国彪
作者单位:1. 江苏华达化工集团,江苏常州,213033
2. 常州大学江苏省精细石油化工重点实验室,江苏常州,213164
摘    要:以L-丙氨酸和四氟化硫为原料,压力下经一步氟化反应制得α-三氟甲基乙胺。实验研究获得的最佳工艺条件为:以100 g L-丙氨酸为原料,n(L-丙氨酸)∶n(四氟化硫)为1∶2,55℃及18-19 kgf/cm^2压力下保温反应12 h,产品收率在55%以上,产品盐酸盐熔点在218.5℃以上。

关 键 词:L-丙氨酸  四氟化硫  氟化反应  α-三氟甲基乙胺

Study on Process for Producing α-Trifluoromethyl Ethylamine
Xu Guanghui,Zhu Guobiao. Study on Process for Producing α-Trifluoromethyl Ethylamine[J]. Guangdong Chemical Industry, 2012, 39(1): 194-195
Authors:Xu Guanghui  Zhu Guobiao
Affiliation:1.Jiangju Huada Chemical Group Co.Ltd.,Changzhou 213033; 2.Changzhou University,Jiangsu Province Key Laboratory of Fine Petrochemicals,Changzhou 213164,China)
Abstract:α-Trifluoromethyl ethylamine was prepared under pressure by using L-alanine and sulfur tetrafluoride as raw materials for one step fluoridation reaction.The optimal operating conditions for the process were investigated experimentally.These conditions obtained are: 100 g of L-alanine as raw material and molecular ratio of sulfur tetrafluoride to L-alanine at 2,the reaction at temperature of 55 ℃ and pressure of 18~19 kgf/cm^2 for 12 h.The yield of the product is above 55 % and the melting point of the hydrochloric salt of the product is above 218.5 ℃.
Keywords:L-alanine  sulfur tetrafluoride  fluoridation  α-Trifluoromethyl ethylamine
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