Search results
Results from the WOW.Com Content Network
Migratory aptitude is the relative ability of a migrating group to migrate in a rearrangement reaction. [1] Migratory aptitudes vary in different reactions, depending on multiple factors. [2] In the Baeyer-Villiger reaction, the more substituted group, in general, migrates. [3] In the pinacol rearrangement, the order of migratory aptitude has ...
The pinacol–pinacolone rearrangement is a method for converting a 1,2-diol to a carbonyl compound in organic chemistry. The 1,2-rearrangement takes place under acidic conditions. The name of the rearrangement reaction comes from the rearrangement of pinacol to pinacolone. [1]
A common migration introduction of carbon is a pinacol rearrangement. [1] While this reaction refers specifically to a vicinal dihydroxide rearrangement, there are other pinacol type rearrangements that proceed through the same general mechanism such as the Tiffeneau–Demjanov rearrangement.
He also discovered what is now known as the pinacol rearrangement, whereby 1,2-diols rearrange to aldehydes or ketones under acid catalysis. [ 4 ] [ 5 ] His work involved the preparation of 2,3-dimethyl-2,3-butanediol ( pinacol ) from acetone , [ 6 ] followed by the rearrangement to 3,3-dimethylbutanone ( pinacolone ), which was then oxidised ...
Most famously, at least in the classroom, pinacolone arises by the pinacol rearrangement, which occurs by protonation of pinacol (2,3-dimethylbutane-2,3-diol). [4] Industrially pinacolone is made by the hydrolysis of 4,4,5-trimethyl-1,3-dioxane, which is the product of isoprene and formaldehyde via the Prins reaction.
Pinacol is a branched alcohol which finds use in organic syntheses. It is a diol that has hydroxyl groups on vicinal carbon atoms. A white solid that melts just above room temperature, pinacol is notable for undergoing the pinacol rearrangement in the presence of acid and for being the namesake of the pinacol coupling reaction .
The reaction is named after pinacol (also known as 2,3-dimethyl-2,3-butanediol or tetramethylethylene glycol), which is the product of this reaction when done with acetone as reagent. The reaction is usually a homocoupling but intramolecular cross-coupling reactions are also possible. Pinacol was discovered by Wilhelm Rudolph Fittig in 1859.
Spiro compounds are often prepared by diverse rearrangement reactions. For example, the pinacol-pinacolone rearrangement is illustrated below. [3]: 985 is employed in the preparation of aspiro[4.5]decane. [12]]. The synthesis of a spiro-keto compound form a symmetrical diol