Barton–McCombie deoxygenation

Theory and Defination :

The Barton–McCombie de-oxygenation is an organic reaction in which an hydroxy functional group in an organic compound is replaced by a hydride to give an alkyl group. It is named for the British chemists Sir Derek Harold Richard Barton (1918–1998) and Stuart W. McCombie.

General Reaction :

This deoxygenation reaction is a radical substitution.

In the related Barton de-carboxylation the reactant is a carboxylic acid.
 

Mechanism :

The reaction mechanism consists of a catalytic radical initiation step and a propagation step. The alcohol (1) is first converted into a xanthate (2). The other reactant tributyltin hydride 3 is decomposed by AIBN 8 into a tributyltin radical 4. The tributyltin radical abstracts the xanthate group from 2 leaving an alkyl radical 5 and tributyltin xanthate (7). The sulfur tin bond in this compound is very stable and provides the driving force for this reaction. The alkyl radical in turn abstracts a hydrogen atom from a new molecule of tributyltin hydride generating the desired deoxygenated product (6) and a new radical species ready for propagation.




Main disadvantage of this reaction is the use of the tin hydride which is toxic, expensive and difficult to remove from the reaction mixture. One alternative is the use of tributyltin oxide as the radical source and poly(methylhydridesiloxane) (PMHS) as the hydride source. Phenyl chlorothionoformate used as the starting material ultimately generates carbonyl sulfide.



Trialkyl boranes

An even more convenient hydrogen donor is provided by trialkylborane-water complexes such as trimethylborane contaminated with small amounts of water.




In this catalytic cycle the reaction is initiated by air oxidation of the trialkylborane 3 by air to the methyl radical 4. This radical reacts with the xanthate 2 to S-methyl-S-methyl dithiocarbonate 7 and the radical intermediate 5. The (CH3)3B.H2O complex 3 provides a hydrogen for recombining with this radical to the alkane 6 leaving behind diethyl borinic acid and a new methyl radical.




It is found by theoretical calculations that that a O-H homolysis reaction in the borane-water complex is endothermic with an energy similar to that of the homolysis reaction in tributyltin hydride but much lower than the homolysis reaction of pure water.

Examples : 

 1)Trapping the radical intermediate is possible when the reacting molecule contains necessary functional groups. An example of intramolecular radical trapping leading to the formation of a five-membered ring is shown below

2)Alkyl xanthates are used commonly, but phenyl thiocarbonates and thiocarbonyl imidazolates are also reactive substrates

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Barton Decarboxylation

Theory and defination :

Barton Decarboxylation is the organic reaction in which the conversion of a carboxylic acid to a thiohydroxamate ester followed by heating the product in the presence of a suitable hydrogen donor such as tri-n-butylin hydride, produces a reductive decarboxylation. This sequence of reaction is called the reaction and may be used to remove a carboxylic acid and replace it with other functional groups.

General Reaction :

An alternative possibility is the introduction of a substituent by reaction with a suitable radical trapping agent:

Mechanism:

The initiation of the Barton Decarboxylation ( Bu3Sn-H -> Bu3Sn. ) is effected with a radical initiator, and as with the Barton-McCombie Deoxygenation, the driving force for the reaction itself is the formation of the stable S-Sn bond.
In addition, Barton esters can also be cleaved photolytically or thermally:

If an excess of a suitable radical trapping agent is present in the reaction medium, substitution will occur; otherwise, radical recombination takes place to give the pyridyl sulfide:

This reaction is named after a British chemist and Nobel Prize laureate Sir Derek Barton.

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