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Abstract

In previous work, a novel pathway for the synthesis of ephedrine/pseudoephedrine and methamphetamine using the precursors benzaldehyde, nitroethane and dimethyl carbonate was investigated, and an impurity profile presented. This paper presents chiral and stable isotope ratios of ephedrine/pseudoephedrine and methamphetamine synthesised by this pathway. Based on the chiral profile and the more negative δ13C (avg. –33.2‰) and more positive δ2H values, it is possible to distinguish ephedrine/pseudoephedrine and methamphetamine prepared from this pathway from those of “fully synthetic”, “semi-synthetic” or “natural” origin. The more positive δ2H values of methamphetamine from this pathway allowed for differentiation from methamphetamine produced from phenyl-2-propanone. It was noted, however, that the use of stable isotope profiling would likely be limited when a benzaldehyde source having a negative δ2H value was used as a precursor. Furthermore, the stable isotope values alone could not be used to differentiate from methamphetamine prepared by the Akabori-Momotani reaction, highlighting the need for combination with impurity profiling.

Details

Title
Profiling ephedrine/pseudoephedrine and methamphetamine synthesised from benzaldehyde, nitroethane and dimethyl carbonate
Author
Miller, Brendan M 1 ; Carter, James F 2 ; Cresswell, Sarah L 3 ; Loughlin, Wendy A 3 ; Culshaw, Peter N 1 

 Forensic Science Queensland, Coopers Plains, QLD 4108, Australia 
 Queensland Health Forensic and Scientific Services, Coopers Plains, QLD 4108, Australia 
 School of Environment and Science, Griffith University, Nathan, QLD 4111, Australia 
Publication year
2024
Publication date
Jul 2024
Publisher
Elsevier Limited
e-ISSN
18726283
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
3065603282
Copyright
©2024. Elsevier B.V.