Department of Chemistry and Center of Excellence for Innovation in Chemistry, Faculty of Science, Mahidol University, Rama VI Road, Bangkok 10400, Thailand.
Org Biomol Chem. 2013 Oct 14;11(38):6650-8. doi: 10.1039/c3ob41247d. Epub 2013 Aug 22.
A general synthesis of γ-trifluoromethyl α,β-unsaturated γ-butyrolactones is described. The fluoride-catalyzed nucleophilic addition of a trifluoromethyl (CF3) group generated from (trifluoromethyl)trimethylsilane (CF3SiMe3, Ruppert-Prakash reagent) to a masked maleic anhydride 1 (cyclopentadiene-maleic anhydride adduct) provides the corresponding adducts 2 with high stereoselectivity. The γ-trifluoromethyl α,β-unsaturated γ-butyrolactones 4 were obtained after treatment of the adducts 2 with Grignard reagents, followed by flash-vacuum pyrolysis.
描述了γ-三氟甲基α,β-不饱和γ-丁内酯的一般合成方法。通过三氟甲基(CF3)基团的氟化物催化亲核加成,该基团由(三氟甲基)三甲基硅烷(CF3SiMe3,Ruppert-Prakash 试剂)生成,与掩蔽的马来酸酐 1(环戊二烯-马来酸酐加合物)发生反应,以高立体选择性提供相应的加合物 2。加合物 2 用格氏试剂处理后,再进行闪蒸真空热解,得到γ-三氟甲基α,β-不饱和γ-丁内酯 4。