Amide formation from acyl chloride | Carboxylic acids and derivatives | Khan Academy

TL;DR

Butanoyl chloride can be converted to the more stable N,N-dimethylbutanamide through a reaction with dimethylamine.

Transcript

Let's think about what might happen if we had a molecule of butanoyl chloride. So one, two, three, four carbons. That's where the but- comes in, and then it's a butanoyl chloride. So it's an acyl halide or it's an acyl chloride. Let me write this down just to give us some practice with namings. This is butanoyl chloride. We saw a couple of videos a... Read More

Key Insights

• 🙅 Butanoyl chloride is an acyl chloride, while N,N-dimethylbutanamide is an amide.
• 👊 The reaction between butanoyl chloride and dimethylamine involves nucleophilic attack and bond rearrangements.
• 🙅 The formation of N,N-dimethylbutanamide is favored because it leads to a more stable carboxylic acid derivative.

Summary & Key Takeaways

• Butanoyl chloride is a carboxylic acid derivative that is less stable than an amide.

• Dimethylamine, a nucleophilic amine, can react with butanoyl chloride to form N,N-dimethylbutanamide.

• The reaction involves the amine attacking the carbonyl carbon, followed by the rearrangement of bonds and formation of a chloride anion.

• The resulting product is N,N-dimethylbutanamide, a more stable carboxylic acid derivative.