Aspirin is generally produced by the following mechanism (starting from basic materials) Phenol --(NaOH, CO2, heat)--> Sodium Salicylate (+para isomer) --(H2SO4)--> Salicylic acid --(acetic anhydride)--> acetylsalicylic acid (Aspirin) Due to the myriad of organic reactions, there are multiple possibilities at each stage. However, the above is the most efficient and common way of synthesizing Aspirin. For example, the last reaction (esterification) may be accomplished by using an acyl halide instead of an anhydride (e.g. ethanoyl/acetic chloride instead of acetic anhydride). However, the acyl halide is more costly to synthesize and more unstable to handle.
yes
diffusion
24 hours
Pyridine is used in the synthesis of aspirin as a catalyst to help facilitate the esterification reaction between salicylic acid and acetic anhydride. Its basic properties help neutralize the acidic byproducts formed during the reaction, which improves the yield of aspirin. Additionally, pyridine can also help dissolve the reactants and promote the formation of the desired product.
Phosphoric acid is used in the synthesis of aspirin as a catalyst to facilitate the esterification reaction between salicylic acid and acetic anhydride. It helps increase the reaction rate and yield of aspirin.
a prostaglandin (PGE2) synthesis inhibitor
No, aspirin synthesis is not an esterification reaction. It involves the reaction of salicylic acid with acetic anhydride to form acetylsalicylic acid (aspirin) and acetic acid through an acetylation reaction. Esterification typically involves the reaction of an alcohol with a carboxylic acid to form an ester.
No. Ibuprofen is derived from propionic acid. Aspirin is acetylsalicylic acid. However, they are both drugs known as NSAIDs and have a common mechanism of action in the body.
Synthesis of acetyl chloride via the reaction of acetic acid with sulphuric acid
Aspirin (acetyl salycilic acid) is prepared from salycilic acid and acetic anhydride; salicylic acid is prepared from sodium phenoxide and carbon dioxide (Kolbe synthesis).
Certain Eicosanoids--M.S. Exercise Physiology
During the synthesis of aspirin, the bonds that break are the ester bonds in acetic anhydride and salicylic acid. New bonds that form are ester bonds between the acetyl group and the hydroxyl group of salicylic acid to produce aspirin.