Divergent thermal behaviour of phenoxymethyl phenyl sulphoxide under gas and condensed-phase conditions

Autor:	Angus R. Brown, Donald K. Cameron, J. I. G. Cadogan, Ian Gosney, Malcolm R. Banks
Rok vydání:	1989
Předmět:	Benzaldehyde chemistry.chemical_compound Anomeric effect Chemistry Radical Yield (chemistry) Thermal decomposition Acetal Organic chemistry Medicinal chemistry Toluene Bond cleavage
Zdroj:	Journal of the Chemical Society, Perkin Transactions 2. :595
ISSN:	1364-5471 0300-9580
DOI:	10.1039/p29890000595
Popis:	A comparison is made between the behaviour of phenoxymethyl phenyl sulphoxide (2) under different thermolytic conditions. Passage of (2) through a quartz tube in the gas phase at 600 °C results in products which can be rationalised by assuming homolytic cleavage of the S–C bond and the generation of both the phenylsulphinyl (4) and phenoxymethyl (6) radicals which decompose by separate pathways to yield S-phenyl benzenethiosulphonate (3) and benzaldehyde, respectively. On the other hand, solution thermolysis of (2) in [2H8]toluene at 110 °C leads to a facile S→O 1,2-shift and the formation of thermally stable phenoxymethyl benzenesulphenate (9) in quantitative yield. A bimolecular oxygen-transfer mechanism is proposed for the conversion of (2) into (9) which is rationalised in terms of a double (stabilising) anomeric effect brought about by the acetal group in (9). Cross-over experiments support the mechanism.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::2dcfa006a1852936a88c94553a6d7b8c https://doi.org/10.1039/p29890000595 Zobrazit plný text záznamu