How is the synthesis of dibenzalacetone carried out?

How is the synthesis of dibenzalacetone carried out?

Synthesis of Dibenzalacetone by Aldol Condensation. 1. To carry out a mixed aldol condensation reaction. 2. To study the mechanism of aldol condensation reaction. The reaction of an aldehyde with a ketone employing sodium hydroxide as the base is an example of a mixed aldol condensation reaction, the Claisen-Schmidt reaction.

How is aldol condensation used to make dibenzalacetone?

Condensation is a process which joins two or more molecules usually with the loss of a small molecule such as water or an alcohol. Aldol condensation (Claisen-Schmidt reaction) definitely is a process which join two carbonyl groups with a loss of water molecule in order to form β-hydroxyketone.

How to recrystallize dibenzalacetone as a solid?

Dibenzalacetone will crash out of the solution as a solid during the course of the reaction. Collect this solid via Hirsch filtration and wash it several times with small portions of cold water. Allow the solid to air dry by continuing to apply the vacuum for 2-3 min. Recrystallize the solid by dissolving in 2 mL of hot ethanol.

How is dibenzalacetone used in sun protection preparations?

Dibenzalacetone is a fairly innocuous substance in which its spectral properties indicate why it is used in sun-protection preparations. In the present experiment, sufficient ethanol is present as solvent to readily dissolve the starting material, benzaldehyde and also the intermediate, benzalacetone.

When was the first synthesis of 1.1.2 indanone?

1.1.2 From acid chlorides: The first synthesis of unsubstituted 1-indanone ( 2 ), obtained from the reaction of phenylpropionic acid chloride with aluminum chloride in benzene (90% yield), has been published in 1927 [24].

How is dibenzal acetone prepared from benzaldehyde and acetone?

To prepare the organic compound Dibenzal acetone from benzaldehyde and acetone in the presence of sodium hydroxide. Aromatic aldehyde undergoes condensation reaction with aldehyde or ketone which contain alpha hydrogen atoms in the presence of an alkali. This reaction is called Claisen-Schmidt reaction.

How to make dibenzalacetone by aldol condensation 49?

Doing the Reaction: 1. Use a 125-mL Erlenmeyer flask with a magnetic stirring bar. 2. Add 50 mL of the NaOH-Ethanol-Water solution mixture. (This was premixed for you.) 3. Place the solution on the magnetic stirrer and adjust the stirring dial to get a nice, even stirring action. 4. To this add the calculated amount of benzaldehyde by syringe 5.