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Iodobenzoic acids are any of three organic compounds with the formula IC 6 H 4 COOH, consisting of a carboxylic acid group and an iodine atom bonded to a central benzene ring. They can be considered as iodinated derivatives of benzoic acid , or as carboxylated variants of iodobenzene .
The synthesis of 2-iodobenzoic acid via the diazotization of anthranilic acid is commonly performed in university organic chemistry labs. One of its most common uses is as a precursor for the preparation of IBX and Dess–Martin periodinane , both used as mild oxidants.
In hot water (or, in Willgerodt's original preparation, steam distillation), iodosobenzene instead disproportionates to iodoxybenzene and iodobenzene: [7] 2 PhIO → PhIO 2 + PhI. 2-Iodobenzoic acid reacts with oxone [8] or a combination of potassium bromate and sulfuric acid to produce the insoluble λ 5 ‑iodane 2-iodoxybenzoic (IBX) acid. [9]
Iodobenzene is commercially available, or it can be prepared in the laboratory from aniline via the diazotization reaction. In the first step, the amine functional group is diazotized with hydrochloric acid and sodium nitrite. Potassium iodide is added to the resultant phenyldiazonium chloride, causing nitrogen gas to evolve. The product is ...
4-iodobenzoic acid crystallization [4] X-ray crystallography of 4-iodobenzoic acid has shown that it crystallizes in the solid state as hydrogen-bonded dimers which stack perpendicular to their aromatic rings. The iodine atoms of adjacent dimers are also oriented towards each other due to van der Waals forces. [4]
This reagent was originally prepared by Conrad Willgerodt [3] by reacting iodobenzene with a mixture of acetic acid and peracetic acid: [4] [5] C 6 H 5 I + CH 3 CO 3 H + CH 3 CO 2 H → C 6 H 5 I(O 2 CCH 3) 2 + H 2 O. PIDA can also be prepared from iodosobenzene and glacial acetic acid: [5] C 6 H 5 IO + 2 CH 3 CO 2 H → C 6 H 5 I(O 2 CCH 3) 2 ...
Iodobenzenes are a group of aryl iodides/halobenzenes consisting of one or more iodine atoms as substituents on a benzene core. They have the formula C 6 H 6–n I n, where n = 1–6 is the number of iodine atoms.
When a substituent group is located ortho position to the carboxyl group in a substituted benzoic acid compound, the compound becomes more acidic surpassing the unmodified benzoic acid. Generally ortho-substituted benzoic acids are stronger acids than their meta and para isomers.