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A re-investigation of the Fries rearrangement of 3-chlorophenyl acetate and synthesis of 2-azido-1-(4-(benzyloxy)-2-chlorophenyl)ethanone from 4-bromo-3-chlorophenol
Tetrahedron Letters ( IF 1.8 ) Pub Date : 2017-11-08 , DOI: 10.1016/j.tetlet.2017.11.016
Panayiotis A. Procopiou , Diane M. Coe , George Procopiou

The Fries rearrangement of 3-chlorophenyl acetate provided the expected 4-chloro-2-hydroxy-acetophenone as the major product and 2,4-diacetyl resorcinol and 2-chloro-4-hydroxy-acetophenone as minor products. 4-Benzyloxy-2-chloroacetophenone was prepared by a Heck reaction and then elaborated to 4-benzyloxy-2-chlorophenacyl azide.



中文翻译:

由4-溴-3-氯苯酚对Fries重排3-氯乙酸苯酯的重新研究和2-叠氮基-1-(4-(苄氧基)-2-氯苯基)乙酮的合成

3-氯苯基乙酸的弗里斯重排提供了预期的4-氯-2-羟基-苯乙酮为主要产物,而2,4-二乙酰基间苯二酚和2-氯-4-羟基-苯乙酮为次要产物。通过Heck反应制备4-苄氧基-2-氯苯乙酮,然后将其精制为4-苄氧基-2-氯苯甲酰基叠氮化物。

更新日期:2017-11-08
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