The Henry reaction is a classic carbon–carbon bond formation reaction in organic chemistry. Discovered in 1895 by the Belgian chemist (1834–1913), it is the combination of a nitroalkane and an aldehyde or ketone in the presence of a base to form β-nitro alcohols. This type of reaction is also referred to as a nitroaldol reaction (nitroalkane, aldehyde, and alcohol). It is nearly analogous to the aldol reaction that had been discovered 23 years prior that couples two carbonyl compounds to form β-hydroxy carbonyl compounds known as "aldols" (aldehyde and alcohol). The Henry reaction is a useful technique in the area of organic chemistry due to the synthetic utility of its corresponding products, as they can be easily converted to other useful synthetic intermediates. These conversions include subsequent dehydration to yield nitroalkenes, oxidation of the secondary alcohol to yield α-nitro ketones, or reduction of the nitro group to yield β-amino alcohols.
center|600px|Henry reaction synthetic scheme
Many of these uses have been exemplified in the syntheses of various pharmaceuticals including the β-blocker (S)-propranolol, the HIV protease inhibitor Amprenavir (Vertex 478), and construction of the carbohydrate subunit of the anthracycline class of antibiotics, L-Acosamine. Although this structure is nucleophilic both at the deprotonated carbon and at the oxy-anions of the nitro group, the observed result is of the carbon attacking the carbonyl compound. The resulting β-nitro alkoxide is protonated by the conjugate acid of the base that originally deprotonated the nitroalkyl structure, giving the respective β-nitro alcohol as product.
center|350px|Henry reaction mechanism
All steps of the Henry reaction are reversible. This is due to the lack of a committed step in the reaction to form product. It is for this reason that research has been geared towards modifications to drive the reaction to completion.
center|500px|Henry stereoselection without modification
Due to the reversibility of the reaction and the tendency for easy epimerization of the nitro-substituted carbon atom (among a number of factors), the Henry reaction will typically produce a mixture of enantiomers or diastereomers. It is for this reason that explanations for stereoselectivity remain scarce without some modification of the reaction. One of the most frequently employed methods for inducing enantio- or diastereoselectivity in the Henry reaction is the use of chiral metal catalysts, in which the nitro group and carbonyl oxygen coordinate to a metal that is bound to a chiral organic molecule. Some metals that have been used include zinc, cobalt, copper, magnesium, and chromium.
Perhaps one of the most synthetically useful modifications to the Henry reaction is the use of an organocatalyst. The catalytic cycle is shown below.
center|500px|Henry reaction synthetic scheme
Benjamin List described that while this is a broad explanation, his brief review illustrates that this is a plausible mechanistic explanation for almost all reactions that involve an organocatalyst. An example of this type of reaction is illustrated in the Examples section of this article.
In addition to the previously mentioned modifications to the Henry reaction there are a variety of others. This includes the conversion of unreactive alkyl nitro compounds to their corresponding dianions which will react faster with carbonyl substrates, reactions can be accelerated using PAP as base, utilization of the reactivity of aldehydes with α,α-doubly deprotonated nitroalkanes to give nitronate alkoxides that yield mainly syn-nitro alcohols once protonated, and finally generation of nitronate anions in which one oxygenatom on the nitro group is silyl-protected to yield anti-β-nitro alcohols in the presence of a fluoride anion source when reacted with an aldehyde.
::center|700px|Acosamine scheme
;Industrial Application
:An enantioselective aldol addition product can be obtained in asymmetric synthesis by reaction of benzaldehyde with nitromethane and the a catalyst system consisting of zinc triflate as a Lewis acid, diisopropylethylamine (DIPEA), and N-methylephedrine (NME) as and as a chiral ligand. A diastereoselective variation of this reaction is depicted below.
::center|500px|Henry reaction application
; Total Synthesis
:In 2005, Barua and coworkers completed the total synthesis of the potent aminopeptidase inhibitor, (–)-bestatin, in an overall yield of 26% overall yield employing Shibasaki's asymmetric Henry reaction as the key step. (illustrated below)
::center|500px|Bestatin
; Organocatalysis
:In 2006, Hiemstra and coworkers explored the use of quinine derivatives as asymmetric catalysts for the reaction between aromatic aldehydes and nitromethane. Through the use of particular derivatives, they were able to induce direct enantioselection through the use of the proper catalyst.
::center|Chinchura
; Biocatalysis
:In 2006, Purkarthofer et al. found that (S)-hydroxynitrile lyase from Hevea brasiliensis catalyzes the formation of (S)-β-nitro alcohols. In 2011, Fuhshuku and Asano showed that the (R)-selective hydroxynitrile lyase from Arabidopsis thaliana could catalyze the synthesis of (R)-β-nitro alcohols from nitromethane and aromatic aldehydes.