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3'-Hydroxyacetophenone CAS:121-71-1 - High-Quality Suppliers and Factory in China for Your Chemical Needs
3-Hydroxyacetophenone has the typical properties of phenolic hydroxyl and carbonyl groups. Phenolic hydroxyl groups have a certain acidity and can react with bases. They can also undergo characteristic reactions of phenols, such as a color reaction with ferric chloride solution to produce a purple color. Carbonyl groups can undergo addition reactions, reduction reactions, etc. For example, they react with hydroxylamine to form oximes, and react with reducing agents such as sodium borohydride to reduce carbonyl groups to hydroxyl groups.
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Chemical Properties
Possesses dual characteristics of phenolic hydroxyl and carbonyl functional groups.
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Reactivity
Exhibits acidity with bases and distinctive purple color reactions with ferric chloride.
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Transformation
Capable of addition and reduction, such as converting to oximes or hydroxyl groups.
Frequently Asked Questions
What are the main functional groups in 3-Hydroxyacetophenone?
3-Hydroxyacetophenone primarily contains phenolic hydroxyl groups and carbonyl groups, which define its chemical behavior.
How does 3-Hydroxyacetophenone react with ferric chloride?
It undergoes a characteristic color reaction with ferric chloride solution, resulting in a distinct purple color.
Can 3-Hydroxyacetophenone react with bases?
Yes, because the phenolic hydroxyl groups possess a certain degree of acidity, the compound can react with various bases.
What happens when 3-Hydroxyacetophenone is treated with sodium borohydride?
Sodium borohydride acts as a reducing agent that reduces the carbonyl groups in 3-Hydroxyacetophenone to hydroxyl groups.
What is formed when it reacts with hydroxylamine?
When 3-Hydroxyacetophenone reacts with hydroxylamine, it undergoes a reaction at the carbonyl group to form oximes.