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三苯基磷系列物的性质如何?

< >我们知道</P> < >1)很多溴代反应中会将三苯基磷加入二氯甲烷中,然后加入溴制成二溴三苯基磷,再同醇反应制备溴代物,</P> < >2)三苯基磷同溴甲烷会生成甲基三苯基溴化磷</P> < >为什么溴代反应可以在二氯甲烷中进行,三苯基磷不同二氯甲烷反应?为什么?(再问三苯基磷同一氯甲烷反应吗?)</P> < >再问Ph3PBr2同醇反应可以制备对应溴代物,不知道Ph3PBr2会不会同甲醇反应?</P> < >知道的请帮忙解释一二,谢谢!</P>
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共4个回答
< >what do you mean (p+进攻羟基),

< >please do not use phases such as (elctrophile attacts nucleophile).

< >indeed, the formation of very strong phosphine oxide double bond is the driving force of the reaction.

< >in most cases, once pph3 and oxygen involved in a reaction o=pph3 would normally be formed as the product.

< >三苯基磷是用来多羟基上的氧的吧,生成的三苯基氧磷很讨厌的,不好除啊 我们都是在乙醚里去掉些在过柱子分出来

以下是引用gentleseven在2008-2-27 23:00:00的发言:
< >what do you mean (p+进攻羟基),

< >please do not use phases such as (elctrophile attacts nucleophile).

< >indeed, the formation of very strong phosphine oxide double bond is the driving force of the reaction.

< >in most cases, once pph3 and oxygen involved in a reaction o=pph3 would normally be formed as the product.

< >" +进攻羟基" is how it wroks. please find the mechanisms of mistsunobu reaction and other reactions where pph3 involved as a reactant. actually if pph3 were that active, it will be much easier for organic chemists to handle many more reactions. [em07][em07][em07]
< >三苯基磷中的p缺电子,所以会同溴化物反应生成溴盐。然后p+进攻羟基,形成p-o键,br-进攻与o相连的c,p-o离去形成三苯氧磷(荧光很强,很难除去),溴代物生成。

< >三苯基磷不跟二氯甲烷反应,可能因为二氯甲烷的活性不够吧。

< >至于ph3pbr2会不会同甲醇反应,动力学上是可能的,只是不知道热力学上能不能实现。

< >一孔之见,希望对你有帮助。谢谢!

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