Synthese und analgetische Wirkung einiger 1‐Methyl‐4‐phenyl‐piperidin‐(4)‐alkylsulfone. 1. Mitteilung

Büchi, J; Prost, M.; Eichenberger, Herbert; Lieberherr, R.

doi:10.1002/hlca.19520350514

Cited by 33 publications

(5 citation statements)

References 7 publications

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“…27 R-d 5 was analogously prepared from R-d benzyl chloride, 28 and the purity was checked by NMR and mass spectroscopy. The sulfoxide (7) 29 and the sulfone (8), 30 as well as the corresponding methoxy-and nitro-substituted derivatives, were prepared by literature methods. Diphenyl sulfoxide and diphenyl sulfone (commercial samples from Aldrich) were purified by chromatography and recrystallization of the central fraction.…”

Section: Discussionmentioning

confidence: 99%

Photosensitized Oxygenation of Benzyl Ethyl Sulfide

et al. 1998

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Singlet oxygen adds to benzyl ethyl sulfide (5, total quenching rate ca. 1 × 107 M-1 s-1, little dependent on the solvent) to ultimately give benzaldehyde (6) and a small amount of the sulfone (8) in aprotic media (rate of the chemical reaction in benzene 5.5 × 106 M-1 s-1) and mainly the sulfoxide (7) in protic media (1.1 × 107 M-1 s-1 in methanol). In the presence of small amounts (0.002−0.3 M) of protic additives (alcohols, phenol, carboxylic acids), the sulfoxide becomes the main product in benzene also. Various evidence support the formation of two intermediates in aprotic solvents. The first one is an exciplex or a syn persulfoxide. It undergoes intramolecular hydrogen abstraction to give a ylide and finally benzaldehyde. Such rearrangement is either a concerted or a radicalic process and not a proton transfer (as indicated by the deuterium effect observed with the α-d benzyl sulfide and the occurrence of the process with the p-nitro and p-methoxy derivatives, 5‘ and 5‘ ‘). This intermediate is not quenched except under relatively strong acidic conditions. A second intermediate, arising either from the first one or through a parallel path, has the properties usually associated with the persulfoxide (possibly it is the anti rotamer). This species gives some sulfoxide but mainly decays to the unreacted sulfide; it can be trapped intermolecularly, however, both by acids and by diphenyl sulfoxide (in the latter case it gives more of sulfone 8 than of sulfoxide 7). The relative rates of protonation of both the first and the second intermediate (determined in benzene doped with protic additives) correlate with the gas-phase acidity of such additives. As for the reaction in neat alcohols and in benzene doped with acids, a single intermediate intervenes. This is better described as a S-hydroperoxy cation rather than a neutral hydroperoxysulfurane and is trapped by both diphenyl sulfoxide and sulfone at rates close to those measured for the photo-oxidation of diethyl sulfide.

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Section: Discussionmentioning

confidence: 99%

Photosensitized Oxygenation of Benzyl Ethyl Sulfide

et al. 1998

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“…Estimation of Thermal Initiation Rate for the Reaction of Styrene with Ethyl Thioglycolate at 80°f Using Mayo's ksi 6. Using Mayo value for pure styrene but assuming second-order initiation.By regarding the ethyl thioglycolate and the product ester as inert diluents, we can calculate…”

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confidence: 99%

The Thermal Reaction of Styrene with Ethyl Thioglycolate; Evidence for the Termolecular Thermal Initiation of Styrene Polymerization

Hiatt¹,

Bartlett²

1959

J. Am. Chem. Soc.

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“…Diallyl sulphide was obtained from Eastman Kodak and was distilled it: vacrro prior to use. Ally1 benzyl sulphide has been prepared previously (27). The remaining compounds were prepared by the condensation of the alkyl mercaptan with allyl bromide, or the alkyl bromide with allyl mercaptan (28).…”

Section: Ally1 Sulplridesmentioning

confidence: 99%