Abstract:
In aqueous polar solvents it is suggested that both pyridinium hydrobromide perbromide and molecular bromine are involved in the bromination of aniline.
Document Type:
Article
Language: English
Citation:
W. Preston Reeves, C. V. Lu, J. S. Russel, “Bromination of Aniline with Pyridinium Hydrobromide Perbromide: some Mechanistic Considerations”, Mendeleev Commun., 4:6 (1994), 223–224
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This publication is cited in the following 5 articles:
Elvira R. Shakurova, Svetlana S. Efimova, Olga S. Ostroumova, Lyudmila V. Parfenova, “One-pot synthesis of quaternary pyridinium salts of lupane triterpenoids and their antimicrobial properties”, New J. Chem., 47:7 (2023), 3347
Shuang Gao, Travis K. Bethel, Tayeb Kakeshpour, Grace E. Hubbell, James E. Jackson, Jetze J. Tepe, “Substrate Controlled Regioselective Bromination of Acylated Pyrroles Using Tetrabutylammonium Tribromide (TBABr3)”, J. Org. Chem., 83:16 (2018), 9250
Indranirekha Saikia, Arun Jyoti Borah, Prodeep Phukan, “Use of Bromine and Bromo-Organic Compounds in Organic Synthesis”, Chem. Rev., 116:12 (2016), 6837
David Bliman, Mariell Pettersson, Mattias Bood, Morten Grøtli, “8-Bromination of 2,6,9-trisubstituted purines with pyridinium tribromide”, Tetrahedron Letters, 55:18 (2014), 2929
W. Preston Reeves, Cuong V. Lu, Brian Schulmeier, Lynette Jonas, Oyvind Hatlevik, “Selective Bromination of Aromatic Ethers with Pyridinium Hydrobromide Perbromide”, Synthetic Communications, 28:3 (1998), 499
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