• Source: Pinacol

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.




Preparation


It may be produced by the pinacol coupling reaction from acetone:




Reactions


As a vicinal-diol, it can rearrange to pinacolone by the pinacol rearrangement, e.g. by heating with sulfuric acid:

Pinacol can be used with borane and boron trichloride to produce useful synthetic intermediates such as pinacolborane, bis(pinacolato)diboron, and pinacolchloroborane.




See also


Pinacol coupling reaction
Pinacol rearrangement
Semipinacol rearrangement




References

Kata Kunci Pencarian:

• Elektrida
• Pinacol
• Pinacol rearrangement
• Pinacol coupling reaction
• Bis(pinacolato)diboron
• Boronic acid
• Prins reaction
• Semipinacol rearrangement
• Hamburg
• Dimethylbutadiene
• Migratory aptitude