How do chemists synthesize anhydrides?

1 Answer
Jun 15, 2016

They use one of two common methods.

Explanation:

You might think that you could form an anhydride by heating a carboxylic acid.

"RCOOH" + "HOCOR" stackrelcolor(blue)(Δcolor(white)(m))(→) "RCO-O-COR" + "H"_2"O"

However, carboxylic acids do not usually lose water by heating.

Chemists therefore use two other methods to synthesize anhydrides.

1. Reaction of carboxylate salts with acyl chlorides

"CH"_3"COONa" + "CH"_3"COCl" stackrelcolor(blue)(Δ)(→) "CH"_3"CO-O-COCH"_3 + "NaCl"

2. Using a dehydrating agent

Chemists can also use dehydrating agents to remove the water from carboxylic acids.

Common dehydrating agents are acetic anhydride, trifluoroacetic anhydride, "PCl"_5, "P"_4"O"_10, and dicyclohexylcarbodiimide (DCC).

"2CH"_3"COOH" + "P"_4"O"_10 → "CH"_3"CO-O-COCH"_3 + "P"_4"O"_9("OH")_2"