摘要
以1-氟萘为起始原料,经卤代、硼酸基团取代卤素以及硼酸基水解3步反应合成重要的医药化工中间体,即标题化合物。该合成方法未见文献报道,原料易得、成本低廉且收率较高。
1-Fluoronaphthalene as a starting material, the important intermediate of 4-fluoro-l-naphthalenol was synthesized via halogen substituted ,boric acid group substituted halogen and the hydrolysis of boric acid group reactions.No reports on the synthe- sis of this compound was found in the literature, and the raw materials was easy to he found, low cost, the total yield was higher.
出处
《化学试剂》
北大核心
2017年第8期895-896,906,共3页
Chemical Reagents
基金
贵州省科技厅社发公关项目(黔科合SY字[2014]3054)
贵州省科技合作项目(黔科合LH字[2016]7442)
关键词
1-氟萘
4-氟-1-萘酚
合成
1-fluoronaphthalene
4-fluoro- 1-naphthalenol
synthesis