2007Chemical engineerRequires access

Technology optimization of cinnamic acid synthesized by knoevenagal reaction using organic alkali catalyst

Jianfen Li

Open publisher page 0 citations

Abstract

Cinnamic acid was synthesized from benzaldehyde and malonic acid as the raw material,and the organic weak-base such as pyridine as the catalyst by Knoevenagel reaction.The main objective of this paper is to improve the synthetic technique of cinnamic acid,reduce the reaction temperature and enhance the yield and purity of the product.Meanwhile,the influence of various weak-base catalysts on yield of cinnamic acid was compared and analyzed. The results indicated that pyridine was the optimal catalyst.Furthermore,in the presence of the organic alkali catalyst,the effects of various technical parameters on the yield of products were investigated by using orthogonal design,and the optimum conditions found for synthesizing cinnamic acid were as follows: pyridine is the optimum catalyst and its amount is 0.02 mol,the molar ratio of benzaldehyde to malonic acid was 1:3,the reaction time was 90min,and the yield reached 90% under these conditions.

About this research paper

What this paper is about

Cinnamic acid was synthesized from benzaldehyde and malonic acid as the raw material,and the organic weak-base such as pyridine as the catalyst by Knoevenagel reaction.The main objective of this paper is to improve the synthetic technique of cinnamic acid,reduce the reaction temperature and enhance the yield and purity of the product.Meanwhile,the influence of various weak-base catalysts on yield of cinnamic acid was compared and analyzed. The results indicated that pyridine was the optimal catalyst.Furthermore,in the presence of the organic alkali catalyst,the effects of various technical parameters on the yield of products were investigated by using orthogonal design,and the optimum conditions found for synthesizing cinnamic acid were as follows: pyridine is the optimum catalyst and its amount is 0.02 mol,the molar ratio of benzaldehyde to malonic acid was 1:3,the reaction time was 90min,and the yield reached 90% under these conditions.

Why it matters

A significance statement is not available in the OpenAlex record.

Key contribution

A contribution statement is not available in the OpenAlex record.

Method / approach

Method details are not available in the OpenAlex metadata.

Main findings

Findings are not separately available in the OpenAlex metadata.

Limitations

Limitations are not available in the OpenAlex metadata.

Applications

Application details are not available in the OpenAlex metadata.

Available abstract

Cinnamic acid was synthesized from benzaldehyde and malonic acid as the raw material,and the organic weak-base such as pyridine as the catalyst by Knoevenagel reaction.The main objective of this paper is to improve the synthetic technique of cinnamic acid,reduce the reaction temperature and enhance the yield and purity of the product.Meanwhile,the influence of various weak-base catalysts on yield of cinnamic acid was compared and analyzed. The results indicated that pyridine was the optimal catalyst.Furthermore,in the presence of the organic alkali catalyst,the effects of various technical parameters on the yield of products were investigated by using orthogonal design,and the optimum conditions found for synthesizing cinnamic acid were as follows: pyridine is the optimum catalyst and its amount is 0.02 mol,the molar ratio of benzaldehyde to malonic acid was 1:3,the reaction time was 90min,and the yield reached 90% under these conditions.

Key concepts: Catalysis, Cinnamic acid, Yield (engineering), Benzaldehyde, Pyridine, Knoevenagel condensation, Chemistry, Malonic acid

Related papers

Back to paper searchBrowse research topicsOriginal source
Technology optimization of cinnamic acid synthesized by knoevenagal reaction using organic alkali catalyst — Research Paper | ScholarLens