2-Iodoxybenzoic acid

IBX can be prepared in a single step by adding an excess of oxone to an aqueous solution of 2-iodobenzoic acid. After warming the solution to 70°C for three hours, the precipitated IBX is collected as a white crystalline solid (80% yield, ≥95% purity). Decomposition of IBX to 2-iodosobenzoic acid and 2-iodobenzoic acid occurs at elevated temperatures, and therefore purification by recrystallization from water is not possible. Purity can be increased (≥99%) by shorting the reaction time to one hour at 70°C, at the cost of slightly reducing yield to 77%.{{ cite journal | title = A User-Friendly Entry to 2-Iodoxybenzoic Acid (IBX) |author1=Frigerio, M. |author2=Santagostino, M. |author3=Sputore, S. | journal = Journal of Organic Chemistry | year = 1999 | volume = 64 | issue = 12 | pages = 4537–4538 | doi = 10.1021/jo9824596 }}

File:IBX Preparation.png{{clear-left}}

The reaction mechanism for an oxidation of an alcohol to an aldehyde according to the hypervalent twisting mechanism{{ cite journal | title = Enhancing 2-Iodoxybenzoic Acid Reactivity by Exploiting a Hypervalent Twist |author1=Su, J. T. |author2=Goddard, W. A. III | journal = Journal of the American Chemical Society | year = 2005 | volume = 127 | issue = 41 | pages = 14146–14147 | doi = 10.1021/ja054446x | pmid = 16218584 |bibcode=2005JAChS.12714146S |url=https://authors.library.caltech.edu/76780/2/ja054446xsi20050824_011746.pdf }} involves a ligand exchange reaction replacing the hydroxyl group by the alcohol followed by a twist and an elimination reaction. The twist is a requirement because the iodine to oxygen double bond is oriented out of plane with the alkoxy group and the concerted elimination would not be able to take place. This twist reaction is a rearrangement in which the oxygen atom is moved into a proper plane for a 5 membered cyclic transition state in the elimination reaction and is calculated by Computational chemistry to be the rate-determining step in the oxidation. The twist mechanism also explains why oxidation is faster for larger alcohols than for small alcohols. The twist is driven forward by the steric hindrance that exists between the ortho hydrogen atom and the protons from the alkoxy group and larger alkoxy groups create larger steric repulsion. The same computation predicts a much faster reacting IBX derivative with a 100 fold reaction rate when this ortho hydrogen atom is replaced by a methyl group thus facilitating the twist until the elimination reaction takes prevalence as the rate determining step.

Image:IBX-Oxidation 2a.svg during conversion of methanol to formaldehyde: a) ligand exchange reaction (activation energy 9.1 kcal/mol (38 kJ/mol), b) hypervalent twist 12.1 kcal/mol (51 kJ/mol), c) elimination 4.7 kcal/mol (20 kJ/mol)).]]{{clear-left}}

IBX exists as two tautomers, one of which is the carboxylic acid. The acidity of IBX which has been determined in water (pKa 2.4) and DMSO (pKa 6.65){{ cite journal | title = o-Iodoxybenzoic Acid (IBX): pK_a and Proton-Affinity Analysis |author1=Gallen, M. J. |author2=Goumont, R. |author3=Clark, T. |author4=Terrier, F. |author5=Williams, C. M. | journal = Angewandte Chemie International Edition | year = 2006 | volume = 45 | issue = 18 | pages = 2929–2934 | doi = 10.1002/anie.200504156 | pmid = 16566050| doi-access = free }} is known to affect organic reactions, for instance acid-catalyzed isomerization accompanying oxidations.

IBX is also available as silica gel or polystyrene bound IBX. In many applications, IBX is replaced by Dess–Martin periodinane which is more soluble in common organic solvents. A sample reaction is an IBX oxidation used in the total synthesis of eicosanoid:{{ cite journal | author1 = Mohapatra, D. K. | author2 = Yellol, G. S. | title = Asymmetric Total Synthesis of Eicosanoid | journal = Arkivoc | year = 2005 | volume = 2005 | issue = 3 | pages = 144–155 | doi = 10.3998/ark.5550190.0006.316 | doi-access = free| hdl = 2027/spo.5550190.0006.316 | hdl-access = free }} More and Finney{{cite journal |last1=More |first1=J.D. |last2=Finney |first2=N.S. |title=A Simple and Advantageous Protocol for the Oxidation of Alcohols with o-Iodoxybenzoic Acid (IBX) |journal=Organic Letters |date=2002 |volume=4 |issue=17 |pages=3001–3003 |doi=10.1021/ol026427n|pmid=12182609}} and Van Arman{{cite journal |last1=Van Arman |first1=S |title=2-Methyl-2-propanol as solvent for o-iodoxybenzoic acid (IBX) oxidation of 1˚ alcohols to aldehydes |journal=Tetrahedron Letters |date=2009 |volume=50 |issue=33 |pages=4693–4695 |doi=10.1016/j.tetlet.2009.06.045 }} have demonstrated that common organic solvents are suitable for many IBX oxidations, despite its low solubility, and in fact may simplify product purification.

:Image:IBXacid example.svg to aldehyde, 94% chemical yield (Mohapatra, 2005)]]{{clear-left}}

In 2001, K. C. Nicolaou and co-workers published a series of papers in the Journal of the American Chemical Society demonstrating, among other transformations, the use of IBX to oxidize primary and secondary benzylic carbons to aromatic aldehydes and ketones, respectively.{{Cite journal|last1=Nicolaou|first1=K. C.|last2=Montagnon|first2=T.|last3=Baran|first3=P. S.|last4=Zhong|first4=Y.-L.|date=2002-03-01|title=Iodine(V) Reagents in Organic Synthesis. Part 4. o-Iodoxybenzoic Acid as a Chemospecific Tool for Single Electron Transfer-Based Oxidation Processes|journal=Journal of the American Chemical Society|volume=124|issue=10|pages=2245–2258|doi=10.1021/ja012127+|pmid=11878978|bibcode=2002JAChS.124.2245N |issn=0002-7863}} The presence of additional water in the solution is now considered to be an essential part of those oxidations.{{Cite web|website=Blog Syn|title=Secret Ingredient|author=See Arr Oh|date=2013-03-03|url=https://blog-syn.blogspot.com/2013/03/blog-syn-003a-secret-ingredient.html}}

IBX is notable for oxidizing vicinal diols (or glycols) to diketones without cleavage of the carbon-carbon bond,{{ cite journal |author1=Frigerio, M. |author2=Santagostino, M. | title = A Mild Oxidizing Reagent for Alcohols and 1,2-Diols: o-Iodoxybenzoic Acid (IBX) in DMSO | journal = Tetrahedron Letters | year = 1994 | volume = 35 | issue = 43 | pages = 8019–8022 | doi = 10.1016/0040-4039(94)80038-3 }} but oxidative cleavage of glycols to two aldehydes or ketones can occur when modified conditions are used (elevated temperatures or trifluoroacetic acid solvent).{{ cite journal |author1=Moorthy, J. N. |author2=Singhal, N. |author3=Senapati, K. | title = Oxidative Cleavage of Vicinal Diols: IBX can do what Dess–Martin Periodinane (DMP) can | journal = Organic & Biomolecular Chemistry | year = 2007 | volume = 5 | issue = 5 | pages = 767–771 | doi = 10.1039/b618135j | pmid = 17315062 }}

:Image:IBX oxidative cleavage.png

The reaction mechanism for this glycol cleavage is based on initial formation of an adduct between 10-I-4 IBX and DMSO to a 12-I-5 intermediate 3 in which DMSO acts as a leaving group for incoming alcohol 4 to intermediate 5. One equivalent of water is split off forming 12-I-5 spirobicyclic periodinane 6 setting the stage for fragmentation to 7. With hydroxyl alpha protons present, oxidation to the acyloin competes. Trifluoroacetic acid is found to facilitate the overall reaction.

:Image:IBX DMSO oxidative cleavage.png

Kirsch and co-workers were able to hydroxylate keto compounds with IBX in α-position under mild conditions.{{ cite journal | author = Kirsch, S. F. | title = IBX-Mediated α-Hydroxylation of α-Alkynyl Carbonyl Systems. A Convenient Method for the Synthesis of Tertiary Alcohols | journal = Journal of Organic Chemistry | year = 2005 | volume = 70 | issue = 24 | pages = 10210–10212 | doi = 10.1021/jo051898j | pmid = 16292876}} This method could be extended to β-keto esters,{{ cite journal |author1=Kirsch, S. F. |author2=Duschek, A. | title = Novel Oxygenations with IBX | journal = Chemistry: A European Journal | year = 2009 | volume = 15 | issue = 41 | pages = 10713–10717 | doi=10.1002/chem.200901867 |pmid=19760735}} and forms a regioselective way to introduce conjugatively activated unsaturation.{{cite journal|url=https://www.organic-chemistry.org/Highlights/2011/04April.shtm|date=4 April 2011|first=Douglass|last=Taber|title=The Ma Synthesis of (-)-GB 13|at=Discussion of intermediate 2|journal=Organic Chemistry Highlights}}

Bartlett and Beaudry discovered that IBX is a valuable reagent for the transformation of β-hydroxyketones to β-diketones. IBX provides yields superior to both the Swern and Dess–Martin oxidation protocols.{{ cite journal |author1=Bartlett, S.L. |author2=Beaudry, C.M. | title = High Yielding Oxidation of β-Hydroxyketones to β-Diketones Using o-Iodoxybenzoic Acid | journal = Journal of Organic Chemistry | year = 2011 | volume = 76 | issue = 23 | pages = 9852–9855 | doi=10.1021/jo201810c |pmid=22023037 }}

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Category:Iodates

Category:Periodinanes

Category:Iodine heterocycles

Category:Oxygen heterocycles

Category:Reagents for organic chemistry

Category:Oxidizing acids

Category:Heterocyclic compounds with 2 rings