Synthesis of 2-bromomethyl-2, 3-dihydrobenzofurans from 2-allylphenols enabled by organocatalytic activation of N-bromosuccinimide. (7th September 2020)

• Record Type: Journal Article
• Authors: Furst, Carolina G.; Cota, Paulo H. P.; dos Santos Wanderley, Taciano A.; Alberto, Eduardo E.
• Is Part Of: New journal of chemistry. Volume 44:Number 36(2020)
• Page Start: 15677
• Page End: 15684
• Publication Date: 2020-09-07
• Subjects: Chemistry -- Periodicals; Chimie -- Périodiques; 540
• DOI: 10.1039/d0nj03432k
• Languages: English
• ISSNs: 1144-0546

Abstract

Abstract : Activation of NBS in acetic acid and a catalytic amount of DBU promotes an intramolecular oxybromination of 2-allylphenols to produce highly aggregated value and densely functionalized 2-bromomethyl-2, 3-dihydrobenzofurans. Abstract : 2-Bromomethyl-2, 3-dihydrobenzofurans are valuable and highly functionalized compounds that can be obtained by an intramolecular reaction between 2-allylphenols and a bromenium ion source (Br + ). Due to the ineffectiveness of the safe and easy-to-handle brominating agent N -bromosuccinimide (NBS) to deliver the desired products, a catalytic process using a mixture of 1, 8-diazabicyclo[5.4.0]undec-7-ene (DBU) and acetic acid was conceived. We hypothesized that this catalytic system delivers in situ acetyl hypobromite (AcOBr) as the active brominating agent, enabling the conversion of a range of 2-allylphenols with diverse electron densities to the products. The protocol was robust enough to permit the reaction to be scaled up to 10 mmols of starting material. Besides, the functional group interconversion with a 2-bromomethyl-2, 3-dihydrobenzofuran derivative was successfully demonstrated.