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All posts | Subject: Allylbenzenes -> Phenylacetaldehyde(-aldoxime) | Please login to post | |||||
Rhodium (Chief Bee) 11-25-03 13:01 No 473067 |
Allylbenzenes -> Phenylacetaldehyde(-aldoxime) (Rated as: excellent) |
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This procedure makes allylbenzenes good phenethylamine precursors - just reduce the substituted phenylacetaldoxime to the phenetylamine using any known method. The Oxidation of Allylbenzenes by the System RuCl3-NaIO4-PTC Yoshifumi Yuasa; Shiroshi Shibuya; Yoko Yuasa Synth. Commun. 33(22), 3947-3952 (2003) (https://www.rhodium.ws/chemistry/allylbenzene2phenylacetaldehyde.html) DOI:10.1081/SCC-120026319 Abstract Methyleugenol 1a was oxidized to give 3,4-dimethoxyphenylacetaldehyde by the oxidative system containing the RuCl3-NaIO4-phase transfer catalyst. The yield and spectroscopic properties were obtained from the stable acetaldoxim 3a. Furthermore, this oxidation system could be applied to other arylpropenes, thus, safrole, 4-methoxyallylbenzene, allylbenzene, and the corresponding arylacetaldehyde formed. |
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