Acetanilide
The ingredients needed to produce aspirin are salicylic acid and acetic anhydride. Acetic acid is also produced as a byproduct during the chemical reaction.
The formation of aspirin will proceed faster if acetic anhydride is used in place of acetic acid. However, acetic anhydride will hydrolyze in the presence of water to form acetic acid, slowing down the reaction.
Acetanilide can also be synthesized by reacting aniline with acetic anhydride, instead of acetyl chloride. This is known as the Acetic Anhydride Method.
Dichloroacetate can be obtained by chlorinating acetic acid with chlorine gas or through the reaction of acetic anhydride with chlorine in the presence of a catalyst. It can also be synthesized by reacting sodium dichloroacetate with a strong acid.
Dehydration of acetic acid to prepare acetic anhydride occur at 8oo oC.
The balanced equation for the reaction between salicylic acid and acetic anhydride to form aspirin (acetylsalicylic acid) is: salicylic acid + acetic anhydride → aspirin + acetic acid.
The reaction between salicylic acid and acetic anhydride involves the substitution of a hydroxyl group in salicylic acid with an acetyl group from acetic anhydride. This reaction is catalyzed by an acid, typically sulfuric acid, and results in the formation of aspirin and acetic acid as byproducts.
The reaction between methylamine and acetic anhydride results in the formation of N-methylacetamide as the primary product. In this reaction, acetic anhydride reacts with methylamine to form an amide functional group. This reaction is a common method for the synthesis of amides in organic chemistry.
If excess acetic anhydride is not removed from the reaction vessel, it can lead to side reactions or undesired byproducts in the final product. It could also affect the purity of the desired compound and make purification more challenging. Additionally, it can pose safety hazards as acetic anhydride is a corrosive and hazardous chemical.
Acetic anhydride undergoes hydrolysis in the presence of water to form acetic acid and a byproduct, typically a carboxylic acid or alcohol. The reaction is a typical nucleophilic acyl substitution reaction, where water acts as a nucleophile attacking the acetic anhydride to break the anhydride bond and form acetic acid.
The chemical reaction between acetic anhydride and salicylic acid is called esterification. This reaction forms acetylsalicylic acid, which is commonly known as aspirin.
The reaction is: (CH3CO)2O + H2O = 2 CH3COOH
As an anhydride, It can be prepared by dehydrating its acid, i.e. Acetic acid, by strong dessicant such as Tetraphosphorus decaoxide(P4O10) :P4O10 + 12 CH3COOH ----> 4 H3PO4 + 6(CH3CO)2O
The reaction between acetyl chloride and sodium acetate would likely result in the formation of acetic anhydride and sodium chloride. Acetyl chloride would react with the sodium acetate to form acetic anhydride, along with sodium chloride as a byproduct.
Adding a small amount of acetic anhydride helps to facilitate the acetylation reaction with aniline, leading to the formation of acetanilide. The acetic anhydride serves as an acetylating agent that transfers an acetyl group to the amine group of aniline, resulting in the desired product. The use of an excess of acetic anhydride is avoided to prevent side reactions and to optimize the yield of acetanilide.
A reaction between an alcohol and an anhydrid is usually exothermic, so I would say it is.
The balanced chemical equation for the reaction involving acetic anhydride (C4H6O3) is: 2C4H6O3 → 4CH3COOH + (CH3CO)2O