benzal chloride

Side products of the reaction include benzal chloride and benzotrichloride.

It can also be prepared from cinnamaldehyde and benzal chloride.

Most benzal chloride main industrial use is as a precursor to benzaldehyde.

Treatment of benzal chloride with sodium gives stilbene.

Benzylic halides are typically strong alkylating agents, and for this reason benzal chloride is treated as a hazardous compound.

Benzal chloride is an organic compound with the formula CHCHCl.

Keywords: benzal chloride, internal potential, 37Cl/35Cl isotope effect on 1H NMR.

Reaction of PhC with benzal chloride in the presence of potassium t-butoxide affords the 3-alkoxy cyclopropene which coverts to the cyclopropenium ion.

Numerous other methods have been developed, such as the partial oxidation of benzyl alcohol, alkali hydrolysis of benzal chloride, and the carbonylation of benzene.

Benzal chloride is produced by the free radical chlorination of toluene, being preceded in the process by benzyl chloride (CHCHCl) and followed by benzotrichloride (CHCCl):

He successfully defended his PhD thesis on "Über den Einfluß von Substituenten auf die Verseifungsgeschwindigkeit von Benzalchlorid (The Influence of substituents on the saponification rate of benzal chloride)" and graduated with distinction.