Synthesis of 1-acyl-1,2-dihydro-3<i>H</i>-pyrazol-3-ones<i>VIA</i>lewis acid-mediated rearrangement of 3-acyloxypyrazoles
作者:Hiroshi Maruoka、Kenji Yamagata、Fumi Okabe、Yukihiko Tomioka
DOI:10.1002/jhet.5570430408
日期:2006.7
The unusual formation of 1-acyl-1,2-dihydro-3H-pyrazol-3-ones starting from 3-acyloxypyrazoles by Fries-type rearrangement is described. Under normal conditions, acylation of 2,4-dihydro-3H-pyrazol-3-ones 1 and 2 with acid chlorides or anhydrides in the presence of triethylamine gave the corresponding 3-acyloxypyrazoles 3a-f and 4a-f. Treatment of 3a-c and 4a-f with Lewis acid, e.g. titanium(IV) chloride
描述了通过弗里斯类型重排从3-酰氧基吡唑开始的1-酰基-1,2-二氢-3 H-吡唑-3-酮的不寻常形成。在正常条件下,在三乙胺存在下用酰氯或酸酐将2,4-二氢-3 H-吡唑-3-酮1和2酰化,得到相应的3-酰氧基吡唑3a-f和4a-f。用路易斯酸,例如氯化钛(IV)和氯化锡(IV)处理3a-c和4a-f,导致酰基迁移,得到相应的1-酰基-1,2-二氢-3 H-吡唑- 3位5a-c和6a-f。有趣的是,3-酰氧基吡唑3e和3f与氯化锡(IV)的反应提供了相应的锡(IV)配合物8e和8f。