you can say as it contain Phenol ring that is undergoes acetylation process to form -OCOCH3
Phenol is converted to aspirin by adding carboxylic acid and esterifying the alcohol.
This reaction is also called p-Hydroxy methylation of Phenol and phenol is converted into p-hydroxy benzyl alc.
C6H5OH + CH3Cl -----(AlCl3)-----> C6H5OHCH3 + HCl phenol + chloromethane ----> 2-methylphenol C6H5OHCH3 -----(alkaline KMnO4, then acidify with HCl)-----> C6H5OHCOOH 2-methylphenol -----> 2-hydroxybenzenecarboxylic acid C6H5OHCOOH + (CH3CO)2O (ethanoic anhydride) -----(c.H2SO4 catalyst)-----> aspirin (C6H5OCOCH3COOH) + (ethanoic acid) CH3COOH
yes using phenol, a compound that is derived from crude oil.
Some common drugs that contain an aromatic phenol group include aspirin, acetaminophen (paracetamol), ibuprofen, and diclofenac. These drugs are widely used as analgesics and anti-inflammatory agents.
Aspirin (acetyl salycilic acid) is prepared from salycilic acid and acetic anhydride; salicylic acid is prepared from sodium phenoxide and carbon dioxide (Kolbe synthesis).
Cumene can be converted to phenol through a two-step process. First, cumene is oxidized to cumene hydroperoxide using oxygen or air. Then, the cumene hydroperoxide undergoes acid-catalyzed cleavage to produce phenol and acetone.
Anisole can be converted into phenol by using a strong aqueous acid, such as hydrochloric acid, in the presence of water and heat. The acidic conditions will cleave the methoxy group (–OCH3) from the benzene ring, resulting in the formation of phenol. This reaction is known as hydrolysis of an ether.
phenol
The major product obtained from the interaction of phenol with sodium hydroxide and carbon dioxide is sodium phenoxide. This is formed through the reaction between phenol and sodium hydroxide to give sodium phenolate, which further reacts with carbon dioxide to form sodium phenoxide and water.
Simple phenolic resins are condensation polymers formed from phenol and formaldehyde. Therefore, they contain only the elements found in phenol and formaldehyde: carbon, hydrogen, and oxygen. The characteristic bond for a cured phenolic resin is a methylene group, derived from a formaldehyde molecule, joining two aromatic rings derived from two phenol molecules. A wide variety of structural formulas are possible, because resins can be made from a variety of ratios between phenol and formaldehyde.
The derivative of Phenol is Carbolic acid.