Trichloronitromethane with acyl chlorides in the presence of tin(II) chloride: Synthesis of trichloronitro ketones

1995-01-01
Demir, Ayhan Gürbüz
Tanyeli, Cihangir
AKSOY, HAVA
Gulbeyaz, V.
Mahasneh, A.S.
Trichloronitromethane adds to acid chlorides in the presence of tin(II) chloride to yield dichloronitro ketones via a substitution reaction. Reduction and dechlorination of the dichloronitro ketones give dichloroamino alcohols and nitro ketones, respectively, in good yield.
Synthesis
Citation Formats
A. G. Demir, C. Tanyeli, H. AKSOY, V. Gulbeyaz, and A. S. Mahasneh, “Trichloronitromethane with acyl chlorides in the presence of tin(II) chloride: Synthesis of trichloronitro ketones,” Synthesis, no. 9, pp. 1071–1073, 1995, Accessed: 00, 2023. [Online]. Available: https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0029154308&origin=inward.