104-92-7Relevant articles and documents
Dehydroxymethyl Bromination of Alkoxybenzyl Alcohols by Using a Hypervalent Iodine Reagent and Lithium Bromide
Shibata, Ayako,Kitamoto, Sara,Fujimura, Kazuma,Hirose, Yuuka,Hamamoto, Hiromi,Nakamura, Akira,Miki, Yasuyoshi,Maegawa, Tomohiro
, p. 2275 - 2278 (2018)
We describe the dehydroxymethylbromination of alkoxybenzyl alcohol by using a hypervalent iodine reagent and lithium bromide in F 3 CCH 2 OH at room temperature. Selective monobromination or dibromination was possible by adjusting the molar ratios of hypervalent iodine reagent and lithium bromide.
Copper-catalyzed halogenation of arylboronic acids
Zhang, Guangyou,Lv, Guanglei,Li, Liping,Chen, Fan,Cheng, Jiang
, p. 1993 - 1995 (2011)
In this Letter, a copper-catalyzed halogenation of arylboronic acids was described. This reaction tolerates a variety of functional groups, providing aromatic halides with good yields. It represents a facile and mild procedure to aryl halides.
Gold-catalyzed halogenation of aromatics by N-halosuccinimides
Mo, Fanyang,Yan, Jerry Mingtao,Qiu, Di,Li, Fei,Zhang, Yan,Wang, Jianbo
, p. 2028 - 2032 (2010)
(Chemical Equation Presented) Golden bromination: A highly efficient and mild AuCl3-catalyzed bromination of aromatic rings with Nbromosuccinimide (NBS) has been developed. This method works with a low catalyst loading (down to 0.01 mol %) and can be combined with transition metal catalyzed transformations to deliver various aryl products.
Site-specific Bromination of Aromatic Compounds: a Rapid Method for Radiobromine Labelling
Adam, Michael J.,Ruth, Thomas J.,Pate, Brian D.,Hall, Laurance D.
, p. 625 - 626 (1982)
Bromobenzene and -p-bromoanisole have been synthesized in less than 5 min by treatment of the aryltin derivative with ammonium bromide, chloramine-T, and HCl in EtOH-H2O at 0 deg C.
Applications of Selenonium Cations as Lewis Acids in Organocatalytic Reactions
He, Xinxin,Wang, Xinyan,Tse, Ying-Lung (Steve),Ke, Zhihai,Yeung, Ying-Yeung
, p. 12869 - 12873 (2018)
The use of trisubstituted selenonium salts as organic Lewis acids in electrophilic halogenation and aldol-type reactions has been developed. The substrate scope is broad. The reaction conditions are mild and compatible with various functionalities. This study opens a new avenue for the development of nonmetallic Lewis acid catalysis.
Electrophilic cleavage reactions of carbon-silicon bonds in neutral hexacoordinate silicon compounds: diorgano(phtalocyaninato)silicon
Tamao, Kohei,Akita, Munetaka,Kato, Hidehito,Kumada, Makoto
, p. 165 - 180 (1988)
Preparations of diorgano(phtalocyaninato)silicon 1)(R2)> and their reactions with N-bromosuccinimide (NBS), halogens, copper(II) halides, and 3-chloroperbenzoic acid (MCPBA) are reported.The alkyl-silicon bonds are readily cleaved by NBS, halogens, and CuX2 to give the corresponding alkyl halides.The reactivity of aryl-silicon bonds toward NBS and halogen depends greatly on the electronic effect of the substituent on the benzene ring, but these bonds are almost inert to CuX2.The reactivity of the carbon-silicon bond towards NBS cleavage decreases in the order 4-MeOC6H4 > n-C8H17 > 4-MeC6H4 > Ph >> 3-CF3C6H4.Cleavage of alkyl-silicon bonds may involv one-electron transfer from substrate to reagent and alkyl radical intermediates, while the electrophilic aromatic substitution mechanism may operate in the cleavage of aryl-silicon bonds. are stable to MCPBA.
Generation of interhalogen fluorides under mild conditions: A comparison of sluggish and reactive interhalogen fluorides
Shellhamer, Dale F.,Horney, Mark J.,Pettus, Benjamin J.,Pettus, Tobiah L.,Stringer, Joy Merry,Heasley, Victor L.,Syvret, Robert G.,Dobrolsky Jr., John M.
, p. 1094 - 1098 (1999)
Interhalogen fluorides (XF; X = I, Br, or Cl) generated from xenon difluoride (XeF2) or triethylamine trihydrofluoride (TREAT HF) with iodine (I2), N-halosuccinimides (NXS; X = I, Br, or Cl), or alkylhypohalites (ROX; R = CH3 or t-Bu, X = Br or Cl) with alkenes and aromatics are reported. A comparison of the above reactions with other methods reported in the literature to generate interhalogen fluorides is made. Interhalogens generated from direct action of elemental fluorine (F2) or XF3 (X = I, Br, or Cl) with chlorine (Cl2), bromine (Br2), or iodine (I2) give a species that can react with electron-deficient alkenes or aromatics. These reagents are too reactive for electron-rich substrates. Interhalogen fluorides from reagents like NXS or ROX with XeF2 or amine HF are much less reactive and give good yields with electron-rich akenes or aromatics.
Efficient one-pot transformation of aminoarenes to haloarenes using halodimethylisulfonium halides generated in situ
Baik, Woonphil,Luan, Wanqiang,Lee, Hyun Joo,Yoon, Cheol Hun,Koo, Sangho,Kim, Byeong Hyo
, p. 213 - 219 (2005)
Halodimethylsulfonium halide 1, which is readily formed in situ from hydrohaloic acid and DMSO, is a good nucleophilic halide. This activated nucleophilic halide rapidly converts aryldiazonium salt prepared in situ by the same hydrohaloic acid and nitrite ion to aryl chlorides, bromides, or iodides in good yield. The combined action of nitrite ion and hydrohaloic acid in DMSO is required for the direct transformation of aromatic amines, which results in the production of aryl halides within 1 h. Substituted compounds with electron-donating or -withdrawing groups or sterically hindered aromatic amines are also smoothly transformed to the corresponding aromatic halides. The only observed by-product is the deaminated arene (usually 7%). The isolated aryldiazonium salts can also be converted to the corresponding aryl halides using 1. The present method offers a facile, one-step procedure for transforming aminoarenes to haloarenes and lacks the environmental pollutants that usually accompany the Sandmeyer reaction using copper halides.
Sodium nitrite-catalyzed oxybromination of aromatic compounds and aryl ketones with a combination of hydrobromic acid and molecular oxygen under mild conditions
Zhang, Guofu,Liu, Renhua,Xu, Qing,Ma, Lixin,Liang, Xinmiao
, p. 862 - 866 (2006)
A novel and efficient catalytic system for the oxybromination of aromatic compounds and aryl ketones utilizing a combination of aqueous hydrobromic acid and molecular oxygen in the presence of sodium nitrite under mild conditions has been developed. The newly developed catalytic system utilizes cheap and readily available reactants, exhibits high bromine atom economy and releases only innocuous water as the by-product.
An efficient, rapid and regioselective nuclear bromination of aromatics and heteroaromatics with NBS using sulfonic-acid-functionalized silica as a heterogeneous recyclable catalyst
Das, Biswanath,Venkateswarlu, Katta,Krishnaiah, Maddeboina,Holla, Harish
, p. 8693 - 8697 (2006)
A simple, efficient and rapid method has been developed for high-yielding regioselective nuclear monobromination of aromatic and heteroaromatic compounds using NBS in the presence of sulfonic-acid-functionalized silica at room temperature. The catalyst works under heterogeneous conditions and can be recycled.
