Halogenation

"Fluorination" redirects here. For the addition of fluoride to drinking water, see Water fluoridation.

For the addition of chlorine, hypochlorite, etc. to drinking water, see Water chlorination.

In chemistry, halogenation is a chemical reaction that involves the addition of one or more halogens to a compound or material. The pathway and stoichiometry of halogenation depends on the structural features and functional groups of the organic substrate, as well as on the specific halogen. Inorganic compounds such as metals also undergo halogenation.

Organic chemistry

Several pathways exist for the halogenation of organic compounds, including free radical halogenation, ketone halogenation, electrophilic halogenation, and halogen addition reaction. The nature of the substrate determines the pathway. The facility of halogenation is influenced by the halogen. Fluorine and chlorine are more electrophilic and are more aggressive halogenating agents. Bromine is a weaker halogenating agent than both fluorine and chlorine, while iodine is the least reactive of them all. The facility of dehydrohalogenation follows the reverse trend: iodine is most easily removed from organic compounds, and organofluorine compounds are highly stable.

Free radical halogenation

Halogenation of saturated hydrocarbons typically requires free radical pathways. The regiochemistry of the halogenation of alkanes is usually determined by the relative weakness of the C–H bonds. This trend is reflected by the faster reaction at tertiary and secondary positions. Free radical halogenation is used for the industrial production of chlorinated methanes:

CH₄ + Cl₂ → CH₃Cl + HCl

Rearrangement often accompany such free radical reactions.

Addition of halogens to alkenes and alkynes

Unsaturated compounds, especially alkenes and alkynes, add halogens:

RCH=CHR′ + X₂ → RCHX–CHXR′

The addition of halogens to alkenes proceeds via intermediate halonium ions. In special cases, such intermediates have been isolated.

Structure of a bromonium ion

Halogenation of aromatic compounds

Chlorination and bromination

Aromatic compounds are subject to electrophilic halogenation:

RC₆H₅ + X₂ → HX + RC₆H₄X

This reaction typically works well for chlorine and bromine. Often a Lewis acidic catalyst is used, such as ferric bromide. Industrial halogenations are often effected by treating the arome with halogen in the presence of iron metal. the halogen reacts with iron, generating the ferric halide catalyst.

Fluorination

Because fluorine is very reactive, the protocol described above would not be efficient as the aromatic molecule would react destructively with F₂. Therefore, other methods, such as the Balz–Schiemann reaction, must be used to prepare fluorinated aromatic compounds.

Iodination

Iodinations can be conducted with hydrogen iodide in the presence of an oxidising agent that generates I₂.

Other halogenation methods

In the Hunsdiecker reaction, from carboxylic acids are converted to the chain-shortened halide. The carboxylic acid is first converted to its silver salt, which is then oxidized with halogen:

RCO₂Ag + Br₂ → RBr + CO₂ + AgBr

The Sandmeyer reaction is used to give aryl halides from diazonium salts, which are obtained from anilines. In the Hell–Volhard–Zelinsky halogenation, carboxylic acids are alpha-halogenated.

In oxychlorination, the combination of hydrogen chloride and oxygen serves as the equivalent of chlorine, as illustrated by this route to dichloroethane:

2 HCl + CH₂=CH₂ + 1⁄2 O₂ → ClCH₂CH₂Cl + H₂O

Halogenation by halogen type

Fluorination

Organic compounds, saturated and unsaturated alike, react readily, usually explosively, with fluorine. Fluorination with elemental fluorine (F₂) requires highly specialised conditions and apparatus. Many commercially important organic compounds are fluorinated electrochemically using hydrogen fluoride as the source of fluorine. The method is called electrochemical fluorination. Aside from F₂ and its electrochemically generated equivalent, a variety of fluorinating reagents are known such as xenon difluoride and cobalt(III) fluoride.

Chlorination

See also: Photochlorination

Chlorination is generally highly exothermic. Both saturated and unsaturated compounds react directly with chlorine, the former usually requiring UV light to initiate homolysis of chlorine. Chlorination is conducted on a large scale industrially; major processes include routes to 1,2-dichloroethane (a precursor to PVC), as well as various chlorinated ethanes, as solvents.

Bromination

Bromination is more selective than chlorination because the reaction is less exothermic. Most commonly bromination is conducted by the addition of Br₂ to alkenes. An example of bromination is the organic synthesis of the anesthetic halothane from trichloroethylene:

Organobromine compounds are the most common organohalides in nature. Their formation is catalyzed by the enzyme bromoperoxidase which utilizes bromide in combination with oxygen as an oxidant. The oceans are estimated to release 1–2 million tons of bromoform and 56,000 tons of bromomethane annually.

Iodination

Iodine is the least reactive halogen and is reluctant to react with most organic compounds. The addition of iodine to alkenes is the basis of the analytical method called the iodine number, a measure of the degree of unsaturation for fats. The iodoform reaction involves degradation of methyl ketones.

Inorganic chemistry

All elements aside from argon, neon, and helium form fluorides by direct reaction with fluorine. Chlorine is slightly more selective, but still reacts with most metals and heavier nonmetals. Following the usual trend, bromine is less reactive and iodine least of all. Of the many reactions possible, illustrative is the formation of gold(III) chloride by the chlorination of gold. The chlorination of metals is usually not very important industrially since the chlorides are more easily made from the oxides and the hydrogen halide. Where chlorination of inorganic compounds is practiced on a relatively large scale is for the production of phosphorus trichloride and sulfur monochloride.

See also

• Dehalogenation
• Haloalkane (Alkyl halide)
• Halogenoarene (Aryl halide)
• Free radical halogenation
• Haloketone
• Electrophilic substitution