Issue 8, 2004

Reversible in situ acid formation for β-pinene hydrolysis using CO2 expanded liquid and hot water

Abstract

Large amounts of waste may result from the neutralization of homogeneous acid catalysts following reaction. Here we present examples of in situ acid formation and self-neutralization, thus eliminating waste and offering advantages for product recovery. The formation of α-terpineol (2) from β-pinene (1) is a reaction of commercial significance that is typically run with strong acid. We demonstrate that the reaction can be performed under more environmentally benign conditions using the in situ acid formation capabilities of two different green technologies: CO2 expanded liquids and reactions in hot water (200 °C). This work presents an example of the application of these methods to a reaction that has commercial significance and adds to our knowledge about the benefits and effects of co-solvents. The relative rates and product distributions achieved in each system are presented and discussed.

Graphical abstract: Reversible in situ acid formation for β-pinene hydrolysis using CO2 expanded liquid and hot water

Article information

Article type
Paper
Submitted
13 Jan 2004
Accepted
05 Apr 2004
First published
26 Apr 2004

Green Chem., 2004,6, 382-386

Reversible in situ acid formation for β-pinene hydrolysis using CO2 expanded liquid and hot water

T. S. Chamblee, R. R. Weikel, S. A. Nolen, C. L. Liotta and C. A. Eckert, Green Chem., 2004, 6, 382 DOI: 10.1039/B400393D

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