Boron tribromide


Boron tribromide, BBr3, is a colorless, fuming liquid compound containing boron and bromine. Commercial samples usually are amber to red/brown, due to weak bromine contamination. It is decomposed by water and alcohols.

Chemical properties

Boron tribromide is commercially available and is a strong Lewis acid.
It is an excellent demethylating or dealkylating agent for the cleavage of ethers, also with subsequent cyclization, often in the production of pharmaceuticals.
The mechanism of dealkylation of tertiary alkyl ethers proceeds via the formation of a complex between the boron center and the ether oxygen followed by the elimination of an alkyl bromide to yield a dibromoborane.
Aryl methyl ethers, on the other hand are dealkylated through a bimolecular mechanism involving two BBr3-ether adducts.
The dibromoborane can then undergo hydrolysis to give a hydroxyl group, boric acid, and hydrogen bromide as products.
It also finds applications in olefin polymerization and in Friedel-Crafts chemistry as a Lewis acid catalyst.
The electronics industry uses boron tribromide as a boron source in pre-deposition processes for doping in the manufacture of semiconductors.
Boron tribromide also mediates the dealkylation of aryl alkyl ethers, for example demethylation of 3,4-dimethoxystyrene into 3,4-dihydroxystyrene.

Synthesis

The reaction of boron carbide with bromine at temperatures above 300 °C leads to the formation of boron tribromide. The product can be purified by vacuum distillation.

History

The first synthesis was done by M. Poggiale in 1846 by reacting boron trioxide with carbon and bromine at high temperatures:
An improvement of this method was developed by F. Wöhler and Deville in 1857. By starting from amorphous boron the reaction temperatures are lower and no carbon monoxide is produced:

Applications

Boron tribromide is used in organic synthesis, pharmaceutical manufacturing, image processing, semiconductor doping, semiconductor plasma etching, and photovoltaic manufacturing.