Organobromine compound

Organobromine compounds are organic compounds that contain carbon bonded to bromine. The most pervasive is the naturally produced bromomethane. One prominent application is the use of polybrominated diphenyl ethers as fire-retardants. A variety of minor organobromine compounds are found in nature, but none are biosynthesized or required by mammals. Organobromine compounds have fallen under increased scrutiny for their environmental impact.

General properties

Most organobromine compounds, like most organohalide compounds, are relatively nonpolar. Bromine is more electronegative than carbon (2.8 vs 2.5). Consequently, the carbon in a carbon–bromine bond is electrophilic, i.e. alkyl bromides are alkylating agents.

Carbon–halogen bond strengths, or bond dissociation energies are of 115, 83.7, 72.1, and 57.6 kcal/mol for bonded to fluorine, chlorine, bromine, or iodine, respectively.[1]

The reactivity of organobromine compounds resembles but is intermediate between the reactivity of organochlorine and organoiodine compounds. For many applications, organobromides represent a compromise of reactivity and cost. The principal reactions for organobromides include dehydrobromination, Grignard reactions, reductive coupling, and nucleophilic substitution.

Synthetic methods

From bromine

Alkenes reliably add bromine without catalysis to give the vicinal dibromides:

RCH=CH2 + Br2 → RCHBrCH2Br

Aromatic compounds undergo bromination simultaneously with evolution of hydrogen bromide. Catalysts such as AlBr3 or FeBr3 are needed for the reaction to happen on aromatic rings. Chlorine-based catalysts (FeCl3, AlCl3) could be used, but yield would drop slightly as dihalogens(BrCl) could form. The reaction details following the usual patterns of electrophilic aromatic substitution:

RC6H5 + Br2 → RC6H4Br + HBr

A prominent application of this reaction is the production of tetrabromobisphenol-A from bisphenol-A.

Free-radical substitution with bromine is commonly used to prepare organobromine compounds. Carbonyl-containing, benzylic, allylic substrates are especially prone to this reactions. For example, the commercially significant bromoacetic acid is generated directly from acetic acid and bromine in the presence of phosphorus tribromide catalyst:

CH3CO2H + Br2 → BrCH2CO2H + HBr

Bromine also converts fluoroform to bromotrifluoromethane.

From hydrogen bromide

Hydrogen bromide adds across double bonds to give alkyl bromides, following the Markovnikov rule:

RCH=CH2 + HBr → RCHBrCH3

Under free radical conditions, the direction of the addition can be reversed. Free-radical addition is used commercially for the synthesis of 1-bromoalkanes, precursors to tertiary amines and quaternary ammonium salts. 2-Phenethyl bromide (C6H5CH2CH2Br) is produced via this route from styrene.

Hydrogen bromide can also be used to convert alcohols to alkyl bromides. This reaction, that must be done under low temperature conditions, is employed in the industrial synthesis of allyl bromide:

HOCH2CH=CH2 + HBr → BrCH2CH=CH2 + H2O

Methyl bromide, another fumigant, is generated from methanol and hydrogen bromide.

From bromide salts

Bromide ions, as provided by salts like sodium bromide, function as a nucleophiles in the formation of organobromine compounds by displacement.[2]

An example of this salt mediated bromide displacement is the use of Copper(II) bromide on ketones:[3][4]

R-CO-CH2-R' + CuBr2 → R-CO-CHBr-R' + CuBr

Industrially significant organobromine compounds

Structure of three industrially significant organobromine compounds. From left: ethylene bromide, bromoacetic acid, and tetrabromobisphenol-A.

Fire-retardants

Organobromine compounds are widely used as fire-retardants.[5] The most prominent member is tetrabromobisphenol-A (4,4'-(1-methylethylidene)bis-(2,6-di-bromophenol, see figure). It and tetrabromophthalic anhydride are precursors to polymers wherein the backbone features covalent carbon-bromine bonds. Other fire retardants, such as hexabromocyclododecane and the bromodiphenyl ethers, are additives and are not chemically attached to the material they protect. The use of organobromine fire-retardants is growing but is also controversial because they are persistent pollutants.

Fumigants and biocides

Ethylene bromide, obtained by addition of bromine to ethylene, was once of commercial significance as a component of leaded gasoline. It was also a popular fumigant in agriculture, displacing 1,2-dibromo-3-chloropropane ("DBCB"). Both applications are declining owing to environmental and health considerations. Methyl bromide is also an effective fumigant, but its production and use are controlled by the Montreal Protocol. Growing in use are organobromine biocides used in water treatment. Representative agents include bromoform and dibromodimethylhydantoin (“DBDMH”).[5] Some herbicides, such as bromoxynil, contain also bromine moieties. Like other halogenated pesticides, bromoxynil is subject to reductive dehalogenation under anaerobic conditions, and can be debrominated by organisms originally isolated for their ability to reductively dechlorinate phenolic compounds.[6]

Dyes

Many dyes contain carbon-bromine bonds. The naturally occurring Tyrian purple (6,6’-dibromoindigo) was a valued dye before the development of the synthetic dye industry in the late 19th century. Several brominated anthroquinone derivatives are used commercially. Bromothymol blue is a popular indicator in analytical chemistry.

Pharmaceuticals

Commercially available organobromine pharmaceuticals include the vasodilator nicergoline, the sedative brotizolam, the anticancer agent pipobroman, and the antiseptic merbromin. Otherwise, organobromine compounds are rarely pharmaceutically useful, in contrast to the situation for organofluorine compounds. Several drugs are produced as the bromide (or equivalents, hydrobromide) salts, but in such cases bromide serves as an innocuous counterion of no biological significance.[5]

Designer drugs

Organobromine compounds such as 4-bromomethcathinone have appeared on the designer drug market alongside other halogenated amphetamines and cathinones in an attempt to circumvent existing drug laws.

Organobromine compounds in nature

Organobromine compounds are the most common organohalides in nature. Even though the concentration of bromide is only 0.3% of that for chloride in sea water, organobromine compounds are more prevalent in marine organisms than organochlorine derivatives. Their abundance reflects the easy oxidation of bromide to the equivalent of Br+, a potent electrophile. The enzyme bromoperoxidase catalyzes this reaction.[7] The oceans are estimated to release 1–2 million tons of bromoform and 56,000 tons of bromomethane annually.[8] Red algae, such as the edible Asparagopsis taxiformis, eaten in Hawaii as "limu kohu", concentrate organobromine and organoiodine compounds in "vesicle cells"; 95% of the essential volatile oil of Asparagopsis, prepared by drying the seaweed in a vacuum and condensing using dry ice, is organohalogen compounds, of which bromoform comprises 80% by weight.[9] Bromoform, produced by several algae, is a known toxin, though the small amounts present in edible algae do not appear to pose human harm.[10] Some of these organobromine compounds are employed in a form of interspecies "chemical warfare." 5-Bromouracil and 3-Bromo-tyrosine have been identified in human white blood cells as products of myeloperoxidase-induced halogenation on invading pathogens.[11]

Structure of some naturally-occurring organobromine compounds. From left: bromoform, a brominated bisphenol, dibromoindigo (Tyrian purple), and the antifeedant tambjamine B.

In addition to conventional brominated natural products, a variety of organobromine compounds result from the biodegradation of fire-retardants. Metabolites include methoxylated and hydroxylated aryl bromides as well as brominated dioxin derivatives. Such compounds are considered persistent organic pollutants and have been found in mammals.

Safety

Alkyl bromine compounds are often alkylating agents and the brominated aromatic derivatives are implicated as hormone disruptors. Of the commonly produced compounds, ethylene dibromide is of greatest concern as it is both highly toxic and highly carcinogenic.

See also

References

  1. ↑ Blanksby SJ, Ellison GB (April 2003). "Bond dissociation energies of organic molecules". Acc. Chem. Res. 36 (4): 255–63. doi:10.1021/ar020230d. PMID 12693923.
  2. ↑ James S. Nowick, Guido Lutterbach, “Sodium Bromide” in Encyclopedia of Reagents for Organic Synthesis John Wiley & Sons, 2001. doi:10.1002/047084289X.rs054
  3. ↑ L. Carroll King; and G. Kenneth Ostrum (1964). "Selective Bromination with Copper(II) Bromide". The Journal of Organic Chemistry 29 (12): 3459–3461. doi:10.1021/jo01035a003.
  4. ↑ Dennis P. Bauer; and Roger S. Macomber (1975). "Iodide catalysis of oxidations with dimethyl sulfoxide. Convenient two-step synthesis of .alpha. diketones from .alpha.-methylene ketones". The Journal of Organic Chemistry 40 (13): 1990–1992. doi:10.1021/jo00901a027.
  5. 1 2 3 David Ioffe, Arieh Kampf “Bromine, Organic Compounds” in Kirk-Othmer Encyclopedia of Chemical Technology 2002 by John Wiley & Sons. doi: 10.1002/0471238961.0218151325150606.a01.
  6. ↑ Cupples, A. M., R. A. Sanford, and G. K. Sims. 2005. Dehalogenation of Bromoxynil (3,5-Dibromo-4-Hydroxybenzonitrile) and Ioxynil (3,5-Diiodino-4-Hydroxybenzonitrile) by Desulfitobacterium chlororespirans. Appl. Env. Micro. 71(7):3741-3746.
  7. ↑ Jayme N. Carter-Franklin, Alison Butler “Vanadium Bromoperoxidase-Catalyzed Biosynthesis of Halogenated Marine Natural Products” Journal of the American Chemical Society 2004, volume 126, 15060-15066. doi:10.1021/ja047925p
  8. ↑ Gordon W. Gribble “The diversity of naturally occurring organobromine compounds” Chemical Society Reviews, 1999, volume 28, pages 335 – 346.doi:10.1039/a900201d
  9. ↑ Rhoda A. Marshall, John T.G. Hamilton , M.J. Dring, D.B. Harper. Do vesicle cells of the red alga Asparagopsis (Falkenbergia stage) play a role in bromocarbon production? Chemosphere 52 (2003) 471–475.
  10. ↑ Agency for Toxic substances and Disease Registry. Bromoform and Dibromochloromethane. Aug 2005. URL: http://www.atsdr.cdc.gov/phs/phs.asp?id=711&tid=128
  11. ↑ Gordon W. Gribble (1998). "Naturally Occurring Organohalogen Compounds". Acc. Chem. Res. 31 (3): 141–152. doi:10.1021/ar9701777.
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