Cyclohexylacetone

From WikiMD's Food, Medicine & Wellness Encyclopedia

Cyclohexylacetone is an organic compound with the formula (CH3)2C(CH2)5COCH3. It is a colorless liquid that is used as a precursor in the synthesis of pharmaceuticals and other organic compounds. This compound is also known as 2-cyclohexyl-2-propanone or 2-ketocyclohexane.

Structure and Properties[edit | edit source]

Cyclohexylacetone is a ketone, a type of organic compound characterized by the presence of a carbonyl group (C=O) in which the carbon atom is covalently bonded to an oxygen atom. The carbon atom of the carbonyl group is also bonded to two other carbon atoms. In the case of cyclohexylacetone, one of these carbon atoms is part of a cyclohexyl group (C6H11), and the other is part of a methyl group (CH3).

The molecular structure of cyclohexylacetone is such that it has a six-membered carbon ring (cyclohexane) with a ketone functional group attached to one of the carbon atoms. This gives the molecule a certain degree of stereochemistry, or three-dimensional structure.

Synthesis[edit | edit source]

Cyclohexylacetone can be synthesized through a variety of methods. One common method involves the reaction of cyclohexanone with acetone in the presence of a base such as sodium hydroxide (NaOH). This reaction is known as an aldol condensation, a type of carbon-carbon bond forming reaction that occurs between two carbonyl compounds.

Uses[edit | edit source]

Cyclohexylacetone is primarily used as a precursor in the synthesis of other organic compounds. It is particularly useful in the pharmaceutical industry, where it can be used to produce a variety of drugs. For example, it can be used in the synthesis of amphetamine-type stimulants.

Safety[edit | edit source]

Like many organic compounds, cyclohexylacetone can be hazardous if not handled properly. It is flammable and can cause irritation if it comes into contact with the skin or eyes. It is recommended to use appropriate safety equipment when handling this compound.


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Contributors: Prab R. Tumpati, MD