Issue 14, 2016

N-Butylpyrrolidinone as a dipolar aprotic solvent for organic synthesis

Abstract

Dipolar aprotic solvents such as N-methylpyrrolidinone (or 1-methyl-2-pyrrolidone (NMP)) are under increasing pressure from environmental regulation. NMP is a known reproductive toxin and has been placed on the EU “Substances of Very High Concern” list. Accordingly there is an urgent need for non-toxic alternatives to the dipolar aprotic solvents. N-Butylpyrrolidinone, although structurally similar to NMP, is not mutagenic or reprotoxic, yet retains many of the characteristics of a dipolar aprotic solvent. This work introduces N-butylpyrrolidinone as a new solvent for cross-coupling reactions and other syntheses typically requiring a conventional dipolar aprotic solvent.

Graphical abstract: N-Butylpyrrolidinone as a dipolar aprotic solvent for organic synthesis

Supplementary files

Article information

Article type
Paper
Submitted
04 Apr 2016
Accepted
26 Apr 2016
First published
26 Apr 2016

Green Chem., 2016,18, 3990-3996

Author version available

N-Butylpyrrolidinone as a dipolar aprotic solvent for organic synthesis

J. Sherwood, H. L. Parker, K. Moonen, T. J. Farmer and A. J. Hunt, Green Chem., 2016, 18, 3990 DOI: 10.1039/C6GC00932H

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