Paper
A new recyclable 1,4-bis(3-methylimidazolium-1-yl)butane ditribromide [bMImB]·(Br3)2 ionic liquid reagent for selective bromination of anilines or phenols and α-bromination of alkanones under mild conditions
Published Jun 13, 2014 · H. Veisi, A. Sedrpoushan, Pourya Mohammadi
RSC Advances
12
Citations
0
Influential Citations
Abstract
1,4-Bis(3-methylimidazolium-1-yl)butane ditribromide [bMImB]·(Br3)2 has been synthesized and explored as a new efficient brominating agent. The crystalline ditribromide reagent is stable for months and acts as a safe source of bromine requiring just 0.5 equiv. for complete bromination. It has a high active bromine content per molecule and shows a remarkable reactivity toward various substrates in acetonitrile at room temperature. The prepared reagents were used as a green recyclable reaction media for the selective bromination of anilines, phenols and α-bromination of alkanones in excellent yields. The product can easily be isolated by just washing the highly water soluble 1,4-bis(3-methylimidazolium-1-yl)butane ditribromide [bMImB]·(Br3)2 from the brominated product. The spent reagent can be recovered, regenerated, and reused without any significant loss.
The new 1,4-bis(3-methylimidazolium-1-yl)butane ditribromide (bMImB)(Br3)2 ionic liquid reagent effectively brominates anilines, phenols, and alkanones under mild conditions, with excellent yield
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