FV-Bromosuccinimide

Radical bromination with fV-bromosuccinimide often succeeds. Thus, 2,5-disubstituted 4-methyloxazoles on bromina-tion give the 4-bromomethyl compounds, and methyl groups at the 4- or 5-positions of isoxazoles 568 and 569 can be brominated with NBS. Controlled mono- or dibromination of 3-aryl-5-methylisoxazole-4-carboxylates allows access to aldehydes <2004T2301>. 

To achieve a clean addition of the elements of hypobromous acid (Br and OH ) it is advantageous to use reagents such as fV-bromosuccinimide 19 as the source of Br in an aqueous medium. So we see, the reactions given in the textbooks to illustrate the characteristic reactivity patterns of functional groups and the synthetic methods elaborated to realize their potential in practice can be vastly different. 

Me-caffeine 8-CH2Br-caffeine fV-Bromosuccinimide (PhC02)2, UV 66AF541... 

Boron trifluoride and boron trifluoride-diethyl ether complex can be used as a source of fluoride ions in the presence of hypobromites and hypochlorites, e.g. methyl hypobromitc, tert-butyl hypobromite, methyl hypochlorite in carbon tetrachloride at 25 C. The addition of bromine monofluoride" and chlorine monofluoride" to various alkenes is accompanied by the formation of the corresponding alkoxybromides and alkoxychlorides which hinder the isolation of the halofluorinated products.57 jV-Bromo- and A -chloro-substiluted alkyl- and arylamines. -amides, and -imides, A -chloro-A,-methylamine, A -bromo-A -methylamine, A -chloro-A, /V-dimethylamine, A-bromo-A.A-dimethylamine, ACV-dichloro-A -methylamine, V,fV-dibromo-,V-mcthylaminc, A -bromosuccinimide, -V-chlorosuccinimide, Af-bromoacct-amide, A.A -dichlorourethane, can be used in the reaction instead of the hypohalites. The reactions with various alkenes conducted in dichloromethane at room temperature in the presence of boron trifluoride-diethyl ether complex produce bromofluoro and chlorofluoro addition products in 40-80 % yield. However, the reactions are complicated by the addition of A -halo-succinimides and Af.A-dichlorourcthane to the C = C bonds.58... 

Treatment of pyrrole, 1-methyl-, 1-benzyl- and 1-phenyl-pyrrole with one mole of Af-bromosuccinimide in THF results in the regiospecific formation of 2-bromopyrroles. Chlorination with fV-chlorosuccinimide is less selective (81JOC2221). Bromination of pyrrole with bromine in acetic acid gives 2,3,4,5-tetrabromopyrrole and iodination with iodine in aqueous potassium iodide yields the corresponding tetraiodo compound. 

---