Reactions of ethyl cinnamates with arylacetamides was written by Shandala, Mowafak Y.;Al-Khashab, Abdul-Ilah Y.;Afzal, M.;Ahmad, Shakir S.. And the article was included in Journal of Heterocyclic Chemistry in 1980.COA of Formula: C10H11FO2 This article mentions the following:
Treating 4-RC6H4CH:CHCO2Et (I; R = H, Cl, Me) with R1C6H4CH2CONH2 (II; R1 = H, 2-, 3-, 4-F, 3-Cl) gave the corresponding 2,6-diketo-3,4-diarylpiperidine III in addition to the corresponding 4-RC6H4CH:CHCONH2 and R1C6H4CH2CO2Et. The latter two are formed from the intermediates of the Claisen condensation of the reactants. Condensation of I (R = MeO) with II gave only p-methoxycinnamide in quant yields with the corresponding arylacetates. In the experiment, the researchers used many compounds, for example, Ethyl 2-(4-fluorophenyl)acetate (cas: 587-88-2COA of Formula: C10H11FO2).
Ethyl 2-(4-fluorophenyl)acetate (cas: 587-88-2) belongs to esters. Esters typically have a pleasant smell; those of low molecular weight are commonly used as fragrances and are found in essential oils and pheromones. Acyl chlorides and acid anhydrides alcoholysis is another way to produce esters. Acyl chlorides and acid anhydrides react with alcohols to produce esters. Anydrous conditions are recommended since both acyl chlorides and acid anhydrides react with water.COA of Formula: C10H11FO2
Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics