当前位置: 首页 > 文章 > 2-氯-5-三氯甲基吡啶合成新方法 农药 2015,54 (12) 868-870+874
Position: Home > Articles > New Synthetic Method of 2-Chloro-5-trichloromethyl Pyridine Agrochemicals 2015,54 (12) 868-870+874

2-氯-5-三氯甲基吡啶合成新方法

作  者:
周俊鹏;吴江;石亚磊;朱锦桃
单  位:
浙江理工大学理学院化学系
关键词:
2-氯-5-三氯甲基吡啶;DL-苹果酸;苯膦酰二氯;催化氯化;合成
摘  要:
[目的]2-氯-5-三氯甲基吡啶是合成农药的重要中间体,开发出一种合成2-氯-5-三氯甲基吡啶的新方法。[方法]以DL-苹果酸为起始原料,通过环化、酯化、氨化、水解生成6-羟基烟酸,后者在苯基膦酰二氯的催化作用下以五氯化磷氯化得到目标产物。[结果]经优化,氯化收率达87%;反应总收率达45.6%(以DL-苹果酸计)。[结论]该路线反应条件温和、操作简单、路线短、产品及中间体易于分离提纯,具有工业化应用前景。
译  名:
New Synthetic Method of 2-Chloro-5-trichloromethyl Pyridine
作  者:
ZHOU Jun-peng;WU Jiang;SHI Ya-lei;ZHU Jin-tao;Department of Sciences,Zhejiang Sci-Tech University;
关键词:
2-chloro-5-trichloromethylpyridine;;DL-Malic acid;;henylphosphonic dichloride;;catalytic chlorination;;synthesis
摘  要:
[Aims] 2-Chloro-5-trichloromethylpyridine is an important insecticide intermediate, this study aims to develop a new method for synthesis of 2-chloro-5-trichloromethylpyridine. [Methods] 6-Hydroxynicotinic acid was obtained from DL-Malic acid as starting material via cyclization, esterification, ammonolysis and hydrolysis. Then it was treated with phosphorus pentachloride under phenylphosphonic dichloride catalysis to give the object product.[Results] The chlorination yield reached 87% under the optimal condition, the total yield was 45.6% based on DL-Malic acid. [Conclusions] The method has advantages of mild reaction condition, simple operation, short routes,all intermediate products are easily purified and identified, which is suitable for industrial production.

相似文章

计量
文章访问数: 10
HTML全文浏览量: 0
PDF下载量: 0

所属期刊

推荐期刊