The addition of "BrF", using N-bromoamides in anhydrous hydrogen fluoride, to a number of aliphatic alkenes has been studied. As expected, the bromine atom in the resultant vicinal fluorobromides exhibited relatively low reactivity in nucleophilic and hydrogenolytic reactions.
已经研究了在无
水氟化氢中使用 N-
溴酰胺将“BrF”添加到许多脂肪族烯烃中。正如预期的那样,所得邻位
氟溴化物中的
溴原子在亲核和氢解反应中表现出相对较低的反应性。