Die Beeinflussung aktiver Methylenverbindungen durch die Nitrogruppe bei der Aminomethinylierung

is much more shielded. The presence of the C-phenyl group in (1) instead of the C-methyl group in (2) has the same effect, since the delocalized aromatic z-electron system of the phenyl group interacts with the vacant p-orbital of the carbene carbon, whose electron deficiency can thus be more effectively lowered than by the methyl group, which only acts inductively[31. Similarly, a dependence between degree of shielding and nature of heteroatom is observed in compounds (3), ( 4 ) , and ( 5 ) . The less electronegative nitrogen in ( 5 ) clearly confers more negative charge on the carbene carbon than does the more strongly electronegative oxygen in (3).In the case of ( 5 ) measurements were carried out on a mixture of the cis-trans isomers [41 (65:35). The isomers, which differ from each other only in the orientation of their C-and N-methyl groups, exhibit different I3C-NMR spectra. The signals for cis-and trans-(5) in the table were assigned on the basis of intensities. The I3C-NMR signals of the two isomers appear in the same sequence as do the N-methyl signals in the 'H-NMR spectrum, oiz. the signal of the cis isomer appears at higher field than that of the trans isomer. -4-phenyl-3-cyclobutene-1,2- We wish to report on the synthesis and properties of 3-mercapto-4-phenyl-3-cyclobutene-1,2-dione (PCB-SH) ( S ) , the first thio analog of the well-known PCB-OHr1I. 3-MercaptoBecause of its expected high acidity and its capability of being transformed into the novel 4-phenyl-3-thiolatocyclobutenediylium 1,2-diolate systemC2], compound ( 5 ) proves to be a very important representative of the phenylcyclobutenedione series.Dropwise addition of a benzene solution of (1) into pyridines (2) saturated with hydrogen sulfide leads to formation of the pyridinium salts ( 3 ) ['I, which have been characterized chemically and spectroscopically (see Table).In agreement with the salt structure, no peaks for the molecular ions appear in the mass spectra of (3a)-(3c). On the other hand, a peak due to the anion whose mass is increased by one unit (m/e 190) and the peak of the cation both appear with high intensity.-The absence of an IR -

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“…2-Aminobenzothiazoles (6) can be converted in an analogous way into the dehydro N-Mannich bases (7).…”

Section: Dehydro N-mannich Bases[***]mentioning

confidence: 99%

“…Reaction of ( 5 ) with phenylsulfenyl chloride leads to the unsymmetrical disulfide (7). ( 4 ) crystals which are readily soluble in methanol, CHCl,, and CH,Cl, and less readily soluble in CC1, and H,O.…”

mentioning

confidence: 98%

3‐Mercapto‐4‐phenyl‐3‐cyclobutene‐1,2‐dione

Schmidt

Reid

Pustolemsek

et al. 1972

Angew. Chem. Int. Ed. Engl.

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Dehydro‐N‐Mannich‐Basen

Kreutzberger

Uzbek

1972

Angewandte Chemie

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are filtered off under suction and recrystallized twice from ethanol; yield 89%, m. p. 156--160°C.( 3 a ) (1.35 g, 5 mmol) is added at room temperature to concentrated hydrochloric acid (25 ml) ; after 3 minutes' stirring the precipitate of ( 5 ) is recovered by filtration (glass suction filter). The crude crop of ( 5 ) is recrystallized from CCl,/CHCl, (or glacial acetic acid); yield 68-75%, m. p.

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Dehydro N‐Mannich Bases

Kreutzberger¹,

Uzbek²

1972

Angew. Chem. Int. Ed. Engl.

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Die Beeinflussung aktiver Methylenverbindungen durch die Nitrogruppe bei der Aminomethinylierung

Cited by 12 publications

References 14 publications

3‐Mercapto‐4‐phenyl‐3‐cyclobutene‐1,2‐dione

3‐Mercapto‐4‐phenyl‐3‐cyclobutene‐1,2‐dione

Dehydro‐N‐Mannich‐Basen

Dehydro N‐Mannich Bases

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