“…81,127 Phenylcopper, lower-and higher-order homocuprates, and lower-and higher-order heterocuprates react with 5a to give aniline in low to moderate yields, at room temperature after 3 h (Scheme 42). …”
“…81,127 Phenylcopper, lower-and higher-order homocuprates, and lower-and higher-order heterocuprates react with 5a to give aniline in low to moderate yields, at room temperature after 3 h (Scheme 42). …”
“…Since cis-azomethane absorbs at 353 nm (9) and 10 and 11 such change as occurs should surely be lowered in the geometry defined by 1 rather than 4 by something like 0.75 eV. 4 An alternative possiblity is that the bands do not represent the same transition, and that relevant bands may be submerged under the other absorption, or be of very low i n t e n~i t y .~ The observation by Arnold and his co-workers (1 3) in a study of five-, six-and seven-membered cyclic 1,4-diaza-1,3-dienes of abnormal spectral changes may be relevant. They found that the long wavelength absorption maximum (normally attributed to an n + x* transition) of 2,3-diphenyl-5,6-dihydropyrazine (12) to be at significantly longer wavelength than either of the related five-or seven-membered equivalents.…”
The synthesis of 3,6-dimethyl-6-n-butyl-5,6-dihydropyridazine, the first 5,6-dihydropyridazine, is described. On heating it undergoes a [1,5] sigmatropic hydrogen rearrangement to give the corresponding 1,6-dihydropyridazine.
weg B: 5.2 g(20 mmol) (10d) (R2= CI&) in 50 ml H20 werden unter Riihren zu 2.07 g (15 mmol) KzCO3 in 10 ml HzO bei 40-45"C getropft. Nach 1 Std. wird die filtrierte Lasung viermal mit je 40 ml Ather extrahiert. Man arbeitet wie unter A auf und erhglt 1.722 g (55 %) gelbe Fliissigkeit, identisch mit nach A dargestelltem (6d).
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