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Thioacetal
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Thioacetal : ウィキペディア英語版
Thioacetal

Thioacetals are the sulfur analogue of acetals. They are prepared in a similar way to acetals: by reacting a thiol with an aldehyde:
:RSH + R'CHO → R'CH(OH)SR
Dithioacetals are prepared similarly to thioacetals, which are intermediates:
:RSH + R'CH(OH)SR → R'CH(SR)2 + H2O
Such reactions typically employ either a Lewis or Brønsted acid catalyst.
Dithioacetals generated from aldehydes and 1,2-ethanedithiol are useful in organic synthesis:
:C2H4(SH)2 + R'CHO → R'CHS2C2H4 + H2O
Whilst the carbonyl carbon of an aldehyde is electrophilic, the ''deprotonated'' derivatives of dithioacetals feature nucleophilic carbon centers:
:R'CHS2C2H4 + R2NLi → R'CLiS2C2H4 + R2NH
Again, this reactivity is most commonly exploited in the 1,3-dithiolanes. The inversion of polarity between R'(H)Cδ+Oδ− and R'CLi(SR)2 is referred to as umpolung.
==See also==

* Thioketal
* Acetal
* Mozingo reduction

抄文引用元・出典: フリー百科事典『 ウィキペディア(Wikipedia)
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