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5α-氯-6β-羟基-雄甾-3,17-二酮的合成
The Synthesis of 5α-Chloro-6β-hydroxy-androst-3,17-dione
【摘要】 以4-雄烯二酮为原料,经羰基保护、双键卤羟化、水解脱保护三步反应合成了5α-氯-6β-羟基-雄甾-3,17-二酮。讨论了保护试剂、催化剂、卤羟化试剂、反应温度等对实验结果的影响,得出了较佳工艺条件,三步总收率达到88%。
【Abstract】 Using 4-androstenedione as raw material, 5α-chloro-6β-hydroxy-androst-3,17-dione was synthesized via carbonyl protection, halogen hydroxylation of double bound and hydrolysis deprotection. The effect of protecting agent, catalyst, halogen hydroxylation agent and temperature were discussed. A better technological condition was obtained with the total yields of 88%.
【关键词】 4-雄烯二酮;
5α-氯-6β-羟基-雄甾-3,17-二酮;
中间体;
【Key words】 4-androstenedione; 5α-chloro-6β-hydroxy-androst-3,17-dion; intermediate;
【Key words】 4-androstenedione; 5α-chloro-6β-hydroxy-androst-3,17-dion; intermediate;
- 【文献出处】 浙江化工 ,Zhejiang Chemical Industry , 编辑部邮箱 ,2014年11期
- 【分类号】O621.3;TQ467
- 【下载频次】66