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(E)-1,1,1-Trifluoro-6,6-bis(4-methoxyphenyl)hexa-3,5-dien-2-one

Laboratorio de Compuestos Organometálicos y Catálisis (Unidad Asociada al CSIC), Departamento de Química Orgánica e Inorgánica, Facultad de Química, Universidad de Oviedo, Julián Clavería 8, E-33006 Oviedo, Spain
Molbank 2020, 2020(1), M1120; https://doi.org/10.3390/M1120
Received: 5 March 2020 / Accepted: 10 March 2020 / Published: 11 March 2020
(This article belongs to the Section Organic Synthesis)
The title compound was obtained in high yield (84%) via the deacetylation of 3-(3,3-bis(4-methoxyphenyl)allylidene)-1,1,1,5,5,5-hexafluoro-2,4-pentanedione with K2CO3 in refluxing methanol. This previously unreported compound has been fully characterized by 19F{1H}, 1H and 13C{1H} NMR, IR, UV-Vis, and HRMS. View Full-Text
Keywords: trifluoromethyl ketones; conjugated dienones; 1,3-butadienes; deacetylation reactions trifluoromethyl ketones; conjugated dienones; 1,3-butadienes; deacetylation reactions
MDPI and ACS Style

Cadierno, V. (E)-1,1,1-Trifluoro-6,6-bis(4-methoxyphenyl)hexa-3,5-dien-2-one. Molbank 2020, 2020, M1120.

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