Abstract
The liquid phase acetolysis of epichlorohydrin (ECH) with acetic acid was studied over bentonite clay catalysts and was found to be very active for the selective formation of 1-acetoxy-3-chloro-2-propanol. The reaction followed first order kinetics with respect to epichlorohydrin and obeyed the Langmuir-Hinshelwood mechanism.
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Selvin, R., Hsu, HL. & Her, TM. Kinetics of regioselective acetolysis of epichlorohydrin. React Kinet Catal Lett 96, 75–82 (2009). https://doi.org/10.1007/s11144-009-5329-7
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DOI: https://doi.org/10.1007/s11144-009-5329-7