Preparation of fluorophenols, fluorohalophenols, N-acylfluoroanilines, and N-acylfluorohaloanilines
申请人:DOWELANCO
公开号:EP0470669A2
公开(公告)日:1992-02-12
Chloro and bromophenols and N-acylanilines are fluorinated in an ortho or para position with an N-fluoropyridinium salt to obtain fluorohalophenols and N-acylfluorohaloanilines, which can be further converted to fluorophenols and N-acylfluoroanilines by reduction. Thus, o-fluorophenol is obtained by fluorination of p-bromophenol with 2-chloro-6-(trichloromethyl)pyridinium fluoroborate and reduction of the product obtained with sodium formate and a palladium catalyst. N-Fluoropyridinium salts having trichloromethyl substituents are disclosed.
氯代和溴代苯酚及 N-酰基苯胺与 N-氟吡啶鎓盐进行正位或对位氟化反应,可得到氟卤苯酚和 N-酰基氟卤苯胺,再通过还原反应将其转化为氟苯酚和 N-酰基氟苯胺。因此,邻氟苯酚是通过对溴苯酚与 2-氯-6-(三氯甲基)吡啶鎓氟硼酸盐氟化,然后用甲酸钠和钯催化剂还原所得到的产物而得到的。本发明公开了具有三氯甲基取代基的 N-氟吡啶鎓盐。