In 1984,Organic Syntheses included an article by Citterio, Attilio. Name: Ethyl 3-(4-chlorophenyl)propanoate. The article was titled 《Reductive arylation of electron-deficient olefins: 4-(4-chlorophenyl)butan-2-one (2-butanone, 4-(4-chlorophenyl)-)》. The information in the text is summarized as follows:
Benzenediazonium compounds 4-RC6H4N2+ (R = H, Br, Cl, OMe, MeCO) were treated with R1CR2:CHR3 (R1 = H, Me, CHMe2, CMe3, Ph; R2 = H, Me; R3 = COMe, CHO, cyano, CO2H, CO2Et) and TiCl3 to yield reductive arylation products I. Thus, CH2:CHCOMe was added to TiCl3 in DMF under N, 4-ClC6H4N2+ Cl- was introduced slowly, and the mixture was stirred to give 4-ClC6H4CH2CH2COMe. In the part of experimental materials, we found many familiar compounds, such as Ethyl 3-(4-chlorophenyl)propanoate(cas: 7116-36-1Name: Ethyl 3-(4-chlorophenyl)propanoate)
Ethyl 3-(4-chlorophenyl)propanoate(cas: 7116-36-1) belongs to organochlorine compounds. The wide structural variety and divergent chemical properties of organochlorides lead to a broad range of names, applications, and properties. Aliphatic organochlorides are often alkylating agents as chlorine can act as a leaving group, which can result in cellular damage.Name: Ethyl 3-(4-chlorophenyl)propanoate
Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics