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Hydroformylation, also known as oxo synthesis, is an important industrial process for the production of aldehydes from alkenes. This chemical reaction entails the addition of a formyl group (CHO) group and a hydrogen atom to a carbon-carbon double bond. This process has witnessed continuous growth since its invention in the 1930’s: production capacity reached 6.6×106 tons in 1995. It is important because the resulting aldehydes are easily converted into many secondary products. For example, in the Shell higher olefin process (SHOP), the resulting aldehydes are hydrogenated to alcohols, which are converted to detergents. Hydroformylation is also used in specialty chemicals, relevant to the organic synthesis of fragrances and natural products. The development of hydroformylation, which originated within the German coal-based industry, is considered one of the premier achievements of 20th century industrial chemistry.
The process typically is accomplished by treatment of an alkene with high pressures (between 10 to 100 atmospheres) of carbon monoxide and hydrogen at temperatures between 40 and 300 °C. Transition metal catalysts are required. When combined with hydrolysis the reaction product is a carboxylic acid in the Koch reaction.
Additional recommended knowledge
The original catalyst was HCo(CO)4, discovered by Otto Roelen. Subsequent work demonstrated that the ligand triphenylphosphine (PPh3) improved the selectivity of the cobalt-catalysed process. Since the 1970’s, most hydroformylation relies on catalysts based on rhodium. Subsequent research led to the development of water-soluble catalysts that facilitate the separation of the products from the catalyst.
The overall mechanism resembles that for homogeneous hydrogenation with additional steps. The reaction begins with the generation of coordinatively unsaturated metal hydrido carbonyl complex such as HCo(CO)3 and HRh(CO)(PPh3)2. Such species bind alkenes, and the resulting complex undergoes a migatory insertion reaction to form a 16 VE alkyl complex.
These isomers result from the differing ways of inserting the alkene into the M-H bond. Of course, both products are not equally desirable. Much research was dedicated to the quest for catalyst that favored the normal isomer.
When the hydrogen is transferred to the carbon bearing the most hydrogen atoms (Markovnikov addition) the resulting alkyl group has a larger steric bulk close to the ligands on the cobalt. If the ligands on the cobalt are bulky (such as tributyl phosphine), then this steric effect is greater. Hence the mixed carbonyl/phosphine complexes offer a greater selectivity towards the straight chain products.
In addition the more electron rich the hydride complex is, the less proton like the hydride is, thus as a result the electronic effects which favour the markovnikov addition to an alkene are less able to direct the hydride to the carbon atom bearing the most hydrogens already. Thus as a result as the metal centre becomes more electron rich the catylst becomes more selective for the straight chain compounds.
After the alkyl formation a second migatory insertion converts the alkyl into an acetyl ligand (this is when the alkyl carbon forms a bond with the carbon of a carbonyl ligand). The vacant site on the metal is filled by two hydrogens (from the oxidative insertion of a hydrogen molecule. One of these hydrides then takes part in a reductive elimination to form the molecule of the aldehyde and the complex [HCo(CO)3].
It is important to note that the rate of migatory insertion of the carbonyl into the carbon-metal bond of the alkyl is fast; in systems where the migatory insertion does not occur (such as nickel hydride tristriphenyl phosphite) the reaction of the hydride with the alkene is reversible. This results in the isomerisation of the alkene, in this way oct-2-ene could be converted into a mixture of both oct-1-ene and oct-2-ene by a beta hydride elimination from the alkyl. In the system below the rate of insertion of the carbonyl carbon into the C-M bond is likely to be greater than the rate of beta-hydride elimination. If the converse was true then some n-C8H17CHO would have been formed.  Hydroformylation of 2-octene: the rhodium catalyst is coordinated to acac and carbon monoxide and encapsulated in a molecular self-assembly process by zinc tetraphenylporphyrin or Zn-tpp and the pyridine analogue of triphenylphosphine. In this process very much like the way enzymes work encapsulation of the catalytic site explains the observed regioselectivity:
Cobalt carbonyl and rhodium complexes catalyse the hydroformylation of formaldehyde and ethylene oxide to give 2-hydroxyacetaldehyde and 3-hydroxypropanaldehyde, which can then be hydrogenated to ethylene glycol and 1,3-propanediol, respectively. The reactions work best when the solvent is basic (such as pyridine). 
In the case of dicobalt octacarbonyl or Co2(CO)8 as a catalyst, 2-pentanone can arise from ethylene and CO, in the absence of hydrogen. A proposed intermediate is the ethylene-propionyl species [CH3C(O)Co(CO)3(ethylene)] which undergoes a migratory insertion to form [CH3COCH2CH2Co(CO)3]. The required hydrogen arises from the water shift reaction. For details see 
If the water shift reaction is not operative, the reaction affords a polymer containing alternating carbon monoxide and ethylene units. Such polymers are more conventionally prepared using palladium catalysts..
|This article is licensed under the GNU Free Documentation License. It uses material from the Wikipedia article "Hydroformylation". A list of authors is available in Wikipedia.|