Issue 7, 2010

An E-factor minimized protocol for the preparation of methyl β-hydroxy esters

Abstract

We report the optimization of the preparation of methyl β-hydroxy esters (3a–l) in 75–93% yield by a solvent-free aldol reaction of aldehydes (1a–l) with KSA (2) followed by a de-silylation step. Amberlite IRA900F and Dowex 50Wx8 H were found to be the most efficient solid catalysts for the aldol addition and de-silylation steps, respectively. In order to minimize the use of organic solvent and automate the recovery of the catalysts and reaction products, we have developed an automated cyclic continuous-flow reactor operating under solvent-free or highly concentrated conditions. This system, applied to the reactions of 1a–c with 2, avoids the mechanical degradation of the catalysts and allowed reduction of the E-factor of the process to a very low value that ranges from 1.41 to 2.09.

Graphical abstract: An E-factor minimized protocol for the preparation of methyl β-hydroxy esters

Supplementary files

Article information

Article type
Paper
Submitted
29 Mar 2010
Accepted
12 May 2010
First published
07 Jun 2010

Green Chem., 2010,12, 1301-1305

An E-factor minimized protocol for the preparation of methyl β-hydroxy esters

F. Fringuelli, D. Lanari, F. Pizzo and L. Vaccaro, Green Chem., 2010, 12, 1301 DOI: 10.1039/C004461J

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