当前位置: X-MOL 学术Beilstein. J. Org. Chem. › 论文详情
Our official English website, www.x-mol.net, welcomes your feedback! (Note: you will need to create a separate account there.)
On the hydrolysis of diethyl 2-(perfluorophenyl)malonate.
Beilstein Journal of Organic Chemistry ( IF 2.7 ) Pub Date : 2020-07-28 , DOI: 10.3762/bjoc.16.153
Ilya V Taydakov 1, 2 , Mikhail A Kiskin 3
Affiliation  

Diethyl 2-(perfluorophenyl)malonate was synthesized in 47% isolated yield by the reaction of sodium diethyl malonate and hexafluorobenzene. The resulting compound was considered as a starting material for synthesizing 2-(perfluorophenyl)malonic acid by hydrolysis. It was found that the desired 2-(perfluorophenyl)malonic acid could not be obtained from this ester by hydrolysis, neither under basic nor under acidic conditions. Nevertheless, hydrolysis of the ester with a mixture of HBr and AcOH gave 2-(perfluorophenyl)acetic acid in a good preparative yield of 63%. A significant advantage of this new approach to 2-(perfluorophenyl)acetic acid is that handling toxic substances such as cyanides and perfluorinated benzyl halides is avoided.

中文翻译:

关于2-(全氟苯基)丙二酸二乙酯的水解。

通过丙二酸二乙酯钠和六氟苯的反应,合成了(全氟苯基)丙二酸二乙酯,分离产率为47%。所得化合物被认为是通过水解合成2-(全氟苯基)丙二酸的原料。已发现,无论是在碱性条件下还是在酸性条件下,都无法通过水解从该酯中获得所需的2-(全氟苯基)丙二酸。然而,用HBr和AcOH的混合物将酯水解,得到63%的良好制备产率的2-(全氟苯基)乙酸。这种新的2-(全氟苯基)乙酸方法的显着优点是避免了处理有毒物质,例如氰化物和全氟苄基卤。
更新日期:2020-07-28
down
wechat
bug