Publication Cover
Synthetic Communications
An International Journal for Rapid Communication of Synthetic Organic Chemistry
Volume 40, 2010 - Issue 6
683
Views
20
CrossRef citations to date
0
Altmetric
Original Articles

Efficient and Regioselective Bromination of Aromatic Compounds with Ethylenebis(N-methylimidazolium) Ditribromide (EBMIDTB)

, , &
Pages 868-876 | Received 17 Mar 2009, Published online: 22 Feb 2010

Keep up to date with the latest research on this topic with citation updates for this article.

Read on this site (3)

Mahboobe Nouzarian, Rahman Hosseinzadeh & Hamid Golchoubian. (2013) Ionic Liquid Iodinating Reagent for Mild and Efficient Iodination of Aromatic and Heteroaromatic Amines and Terminal Alkynes. Synthetic Communications 43:21, pages 2913-2925.
Read now
Madhudeepa Dey & Siddhartha Sankar Dhar. (2012) Synthesis of quaternary ammonium tribromides: a novel green approach. Green Chemistry Letters and Reviews 5:4, pages 639-642.
Read now

Articles from other publishers (17)

Shiv Shankar Gupta, Manisha, Rakesh Kumar, Ankit Kumar Dhiman & Upendra Sharma. (2021) Predictable site-selective functionalization: Promoter group assisted para -halogenation of N -substituted ( hetero ) aromatics under metal-free condition . Organic & Biomolecular Chemistry 19:44, pages 9675-9687.
Crossref
Sourav Mal, Manoranjan Jana & Satinath Sarkar. (2021) Recent Update on Transition Metal‐Free C(sp 2 )−H Bond Halogenation in (Hetero) Arenes . ChemistrySelect 6:41, pages 11299-11330.
Crossref
Matthew Waterford, Simon Saubern & Christian H. Hornung. (2021) Evaluation of a Continuous-Flow Photo-Bromination Using. Australian Journal of Chemistry 74:8, pages 569-573.
Crossref
Jalal Albadi & Mehdi Jalali. (2020) New Procedure for the Highly Regioselective Aerobic Bromination of Aromatic Compounds Using Copper-based Nanocatalyst. Letters in Organic Chemistry 17:3, pages 234-239.
Crossref
Ligeng Wang, Chun Feng, Yan Zhang & Jun Hu. (2020) Regioselective Monobromination of Phenols with KBr and ZnAl–BrO3−–Layered Double Hydroxides. Molecules 25:4, pages 914.
Crossref
Eknath M. Gayakwad, Khushbu P. Patel & Ganapati S. Shankarling. (2019) Sodium sulfate–hydrogen peroxide–sodium chloride adduct: selective protocol for the oxidative bromination, iodination and temperature dependent oxidation of sulfides to sulfoxides and sulfones. New Journal of Chemistry 43:15, pages 6001-6009.
Crossref
Resmin Khatun, Surajit Biswas, Swarbhanu Ghosh & Sk. Manirul Islam. (2018) Polymer-anchored [Fe(III)Azo] complex: An efficient reusable catalyst for oxidative bromination and multi-components reaction for the synthesis of spiropiperidine derivatives. Journal of Organometallic Chemistry 858, pages 37-46.
Crossref
Jimmy C. Kromann, Jan H. Jensen, Monika Kruszyk, Mikkel Jessing & Morten Jørgensen. (2018) Fast and accurate prediction of the regioselectivity of electrophilic aromatic substitution reactions. Chemical Science 9:3, pages 660-665.
Crossref
Pakorn Bovonsombat, Pattaradra Teecomegaet, Panisanun Kulvaranon, Aditi Pandey, Kittithorn Chobtumskul, Sireethorn Tungsirisurp, Punyanuch Sophanpanichkul, Satreerat Losuwanakul, Dechathon Soimaneewan, Patcharida Kanjanwongpaisan, Pornpawit Siricharoensang & Sirirat Choosakoonkriang. (2017) Regioselective monobromination of aromatics via a halogen bond acceptor-donor interaction of catalytic thioamide and N-bromosuccinimide. Tetrahedron 73:46, pages 6564-6572.
Crossref
Shilpa Eshwar Rao & Gayathri Virupaiah. (2017) Oxidative bromination and oxidation of organic substrates catalyzed by bis[2,2'-hydroxyphenylbenzimidazole]Fe(III) complex entrapped in zeolite-Y cavity. Journal of Chemical Technology & Biotechnology 92:8, pages 2060-2074.
Crossref
Indranirekha Saikia, Arun Jyoti Borah & Prodeep Phukan. (2016) Use of Bromine and Bromo-Organic Compounds in Organic Synthesis. Chemical Reviews 116:12, pages 6837-7042.
Crossref
Rahman Hosseinzadeh, Hamid Golchoubian & Mahboobe Nouzarian. (2014) A mild and efficient method for the conversion of aldehydes into nitriles and thiols into disulfides using an ionic liquid oxidant. Research on Chemical Intermediates 41:7, pages 4713-4725.
Crossref
Rahman Hosseinzadeh, Mahmood Tajbakhsh, Mohammad Mavvaji & Zahra Lasemi. (2013) Synthesis of β-aryl vinyl bromides from α, β-unsaturated carboxylic acids by use of ethylenebis(N-methylimidazolium) ditribromide. Research on Chemical Intermediates 41:4, pages 2427-2436.
Crossref
Hojat Veisi, Alireza Sedrpoushan, Pourya Mohammadi, Ali Reza Faraji & Sami Sajjadifar. (2014) A new recyclable 1,4-bis(3-methylimidazolium-1-yl)butane ditribromide [bMImB]·(Br 3 ) 2 ionic liquid reagent for selective bromination of anilines or phenols and α-bromination of alkanones under mild conditions . RSC Adv. 4:49, pages 25898-25903.
Crossref
Lalit Kumar, Tanu Mahajan & Dau Dayal Agarwal. (2012) Aqueous Bromination Method for the Synthesis of Industrially-Important Intermediates Catalyzed by Micellar Solution of Sodium Dodecyl Sulfate (SDS). Industrial & Engineering Chemistry Research 51:5, pages 2227-2234.
Crossref
Lalit Kumar, Tanu Mahajan & D. D. Agarwal. (2011) An instant and facile bromination of industrially-important aromatic compounds in water using recyclable CaBr2–Br2 system. Green Chemistry 13:8, pages 2187.
Crossref
Rahman Hosseinzadeh, Mahmood Tajbakhsh, Maryam Mohadjerani & Zahra Lasemi. (2010) ChemInform Abstract: Efficient and Regioselective Bromination of Aromatic Compounds with Ethylenebis(N‐methylimidazolium) Ditribromide (EBMIDTB).. ChemInform 41:32.
Crossref

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.