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I understand (sort of) that methamphetamine synthesis is often achieved by reducing pseudoephedrine/ephedrine, usually with hi or solvated electrons via the birch reduction, but recently methcathinone synthesis has caught my eye. From what I gather it involves oxidation of the ephedrine/pseudoephedrine. Supposing for research purposes that I have access to some fairly pure and clean ephedrine hcl, what is the safest and easiest way to do this? Iād love to hear your experience and feedback. Thanks in advance.
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