GET THE APP

Comparative study of solid state and solution aldol reaction of l | 43175
Organic Chemistry: Current Research

Organic Chemistry: Current Research
Open Access

ISSN: 2161-0401

+44 1478 350008

Comparative study of solid state and solution aldol reaction of lithium enolate of pinacolone


24th Global Organic & Inorganic Chemistry Conference

July 18-19, 2018 | Atlanta, USA

Huan Pang and Paul G. Williard

Brown University, Providence, USA

Posters & Accepted Abstracts: Organic Chem Curr Res

Abstract :

We reported the first systematic study of the solid-state aldol reactions of lithium pinacolone enolate with various aromatic solid aldehydes, in comparison with the same reactions performed in tetrahydrofuran (THF) solution. In solution, the reactions are selective with the aldol condensation product, except for the reaction involving 2-nitrobenzaldehyde. In the solid state, the reactions with THF-solvated lithium enolate of pinacolone showed the mixture of aldol condensation and aldol addition products. The usage of unsolvated lithium enolate of pinacolone in the solid state reactions resulted in a higher ratio of aldol addition to aldol condensation product than THF-solvated lithium enolate of pinacolone. At lower temperatures (0�?°C), the solid state reactions can afford a higher ratio of aldol addition to aldol condensation product in the system. The solid-state reactions generally afforded low yields and low conversion of the aldehydes. For those aldehydes with halogen group on the para position of benzaldehyde, the Tishchenko product was formed in a large amount in the system catalyzed by lithium enolate of pinacolone (as the strong base).

Biography :

Huan Pang had his Bachelor’s degree in Chemistry in University of Science and Technology of China and now pursues his Chemistry PhD degree at Brown University. He has published 3 papers in reputed journals. Recently, his research topic is focusing on the solid state organolithium chemistry.

E-mail: hzhou15@student.gsu.edu

Top