An article Convenient One-Pot Synthesis of Allylsilanes from Enolizable Ketones WOS:000498684900001 published article about GRIGNARD-REAGENTS; OLEFINATION; ALDEHYDES; SALTS in [Kwan, Man Lung D.; Challen, Paul R.; Tran, Quynh D-D] John Carroll Univ, Dept Chem, 1 John Carroll Blvd, University Hts, PA 44118 USA in 2019.0, Cited 33.0. The Name is 1-(4-Nitrophenyl)ethanone. Through research, I have a further understanding and discovery of 100-19-6. Category: benzodioxans
A convenient one-pot synthesis of allylsilanes from enolizable methyl aryl ketones has been developed. The first step involves nucleophilic addition of the trimethylsilylmethyl group to ketones using the alkylation method developed by Ishihara with slight modification to generate the corresponding beta-silylalkoxides. The second step entails addition of diisobutylaluminum chloride and heating at about 130 degrees C overnight to afford allylsilanes in fair yields.
Category: benzodioxans. About 1-(4-Nitrophenyl)ethanone, If you have any questions, you can contact Kwan, MLD; Challen, PR; Tran, QDD or concate me.
Reference:
Benzodioxan,
,1,4-Benzodioxane | C8H8O2 – PubChem