4-Hydroxyphenylacetone: Difference between revisions
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== 4-Hydroxyphenylacetone == | |||
[[File:4-Hydroxyphenylacetone.svg|thumb|right|Structural formula of 4-Hydroxyphenylacetone]] | |||
'''4-Hydroxyphenylacetone''' is an organic compound with the chemical formula C<sub>9</sub>H<sub>10</sub>O<sub>2</sub>. It is a phenolic ketone and a derivative of [[phenylacetone]]. This compound is of interest in the field of [[organic chemistry]] due to its role as an intermediate in the synthesis of various pharmaceuticals and its occurrence in certain metabolic pathways. | |||
4-Hydroxyphenylacetone | |||
== | == Chemical Structure and Properties == | ||
4-Hydroxyphenylacetone consists of a phenyl ring substituted with a hydroxy group at the para position and an acetone moiety. The presence of the hydroxy group makes it a phenolic compound, which can participate in hydrogen bonding, affecting its solubility and reactivity. | |||
==Biological | === Physical Properties === | ||
4-Hydroxyphenylacetone is a metabolite of certain [[catecholamines]], such as [[dopamine]]. It is involved in the | |||
- '''Molecular Weight:''' 150.18 g/mol | |||
- '''Appearance:''' White to off-white crystalline solid | |||
- '''Solubility:''' Soluble in organic solvents such as ethanol and ether | |||
=== Chemical Properties === | |||
4-Hydroxyphenylacetone can undergo typical reactions of phenols, such as [[electrophilic aromatic substitution]] and [[oxidation]]. The ketone group can participate in reactions like [[nucleophilic addition]] and [[reduction]]. | |||
== Synthesis == | |||
4-Hydroxyphenylacetone can be synthesized through several methods, including the [[Friedel-Crafts acylation]] of phenol with chloroacetone, followed by hydrolysis. Another method involves the oxidation of 4-hydroxyphenyl-2-propanol. | |||
== Biological Role == | |||
In biological systems, 4-Hydroxyphenylacetone is a metabolite of certain [[catecholamines]], such as [[dopamine]]. It is formed through the action of [[monoamine oxidase]] and other enzymes involved in the degradation of neurotransmitters. | |||
== Applications == | |||
4-Hydroxyphenylacetone is used as an intermediate in the synthesis of various [[pharmaceuticals]], including [[antidepressants]] and [[antipsychotics]]. Its ability to undergo further chemical transformations makes it a valuable compound in medicinal chemistry. | |||
== Safety and Handling == | |||
As with many chemical compounds, appropriate safety measures should be taken when handling 4-Hydroxyphenylacetone. It should be stored in a cool, dry place, and contact with skin and eyes should be avoided. | As with many chemical compounds, appropriate safety measures should be taken when handling 4-Hydroxyphenylacetone. It should be stored in a cool, dry place, and contact with skin and eyes should be avoided. | ||
==Related | == Related Pages == | ||
* [[Phenylacetone]] | |||
* [[Phenol]] | * [[Phenol]] | ||
* [[ | * [[Ketone]] | ||
* [[ | * [[Organic chemistry]] | ||
{{Organic compounds}} | |||
[[Category: | [[Category:Phenolic compounds]] | ||
[[Category:Ketones]] | [[Category:Ketones]] | ||
Latest revision as of 16:24, 16 February 2025
4-Hydroxyphenylacetone[edit]
4-Hydroxyphenylacetone is an organic compound with the chemical formula C9H10O2. It is a phenolic ketone and a derivative of phenylacetone. This compound is of interest in the field of organic chemistry due to its role as an intermediate in the synthesis of various pharmaceuticals and its occurrence in certain metabolic pathways.
Chemical Structure and Properties[edit]
4-Hydroxyphenylacetone consists of a phenyl ring substituted with a hydroxy group at the para position and an acetone moiety. The presence of the hydroxy group makes it a phenolic compound, which can participate in hydrogen bonding, affecting its solubility and reactivity.
Physical Properties[edit]
- Molecular Weight: 150.18 g/mol - Appearance: White to off-white crystalline solid - Solubility: Soluble in organic solvents such as ethanol and ether
Chemical Properties[edit]
4-Hydroxyphenylacetone can undergo typical reactions of phenols, such as electrophilic aromatic substitution and oxidation. The ketone group can participate in reactions like nucleophilic addition and reduction.
Synthesis[edit]
4-Hydroxyphenylacetone can be synthesized through several methods, including the Friedel-Crafts acylation of phenol with chloroacetone, followed by hydrolysis. Another method involves the oxidation of 4-hydroxyphenyl-2-propanol.
Biological Role[edit]
In biological systems, 4-Hydroxyphenylacetone is a metabolite of certain catecholamines, such as dopamine. It is formed through the action of monoamine oxidase and other enzymes involved in the degradation of neurotransmitters.
Applications[edit]
4-Hydroxyphenylacetone is used as an intermediate in the synthesis of various pharmaceuticals, including antidepressants and antipsychotics. Its ability to undergo further chemical transformations makes it a valuable compound in medicinal chemistry.
Safety and Handling[edit]
As with many chemical compounds, appropriate safety measures should be taken when handling 4-Hydroxyphenylacetone. It should be stored in a cool, dry place, and contact with skin and eyes should be avoided.
Related Pages[edit]
| Organic compounds | ||||||||||
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This organic compounds related article is a stub.
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