Reversible in situ acid formation for β-pinene hydrolysis using CO2expanded liquid and hot water
- 1 January 2004
- journal article
- Published by Royal Society of Chemistry (RSC) in Green Chemistry
- Vol. 6 (8), 382-386
- https://doi.org/10.1039/b400393d
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.Keywords
This publication has 41 references indexed in Scilit:
- The catalytic opportunities of near-critical water: a benign medium for conventionally acid and base catalyzed condensations for organic synthesisGreen Chemistry, 2003
- In Situ Formation of Alkylcarbonic Acids with CO2The Journal of Physical Chemistry A, 2001
- Comparison of Reversed-Phase HPLC Separation Using Carbon Dioxide and Fluoroform for Enhanced-Fluidity Liquid Mobile PhasesAnalytical Chemistry, 1998
- Alkylation Reactions in Near-Critical Water in the Absence of Acid CatalystsIndustrial & Engineering Chemistry Research, 1997
- Ionic equilibria in aqueous organic solvent mixtures the dissociation constants of acids and salts in tetrahydrofuran/water mixturesAnalytica Chimica Acta, 1997
- Aquathermolysis: Reactions of Organic Compounds with Superheated WaterAccounts of Chemical Research, 1996
- Comparison of Supercritical Fluids and Enhanced-Fluidity Liquids for the Extraction of Phenolic Pollutants from House DustAnalytical Chemistry, 1996
- Solvent expansion and solute solubility predictions in gas‐expanded liquidsAIChE Journal, 1990
- Rearrangements of pinane derivatives. Part V. The influence on rearrangements of a neutral nucleophile associated with the carbonium ionJournal of the Chemical Society, Perkin Transactions 2, 1974
- MonomethylcarbonatAngewandte Chemie, 1972