Latypova, L. R. published the artcileTransformations of 2-Ethyl-2-methyl-2,3-dihydro-1H-indole at the 3-Position, Category: nitriles-buliding-blocks, the main research area is ethyl methyl dihydro indole transformation.
The oxidation of N-acetyl-2-ethyl-2-methyl-2,3-dihydro-1H-indole with pyridinium chlorochromate, CrO3 · 2 Py, or CrO3 gave N-acetyl-2-ethyl-2-methyl-2,3-dihydro-1H-indol-3-one which was hydrolyzed to 2-ethyl-2-methyl-2,3-dihydro-1H-indol-3-one. The latter was reduced with sodium tetrahydridoborate in ethanol to (3RS)-2-ethyl-2-methyl-2,3-dihydro-1H-indol-3-ol and converted to the corresponding 2-ethyl-N-hydroxy-2-methyl-2,3-dihydro-1H-indol-3-imine by treatment with hydroxylamine hydrochloride in methanol. Baeyer-Villiger oxidation of 2-ethyl-2-methyl-2,3-dihydro-1H-indol-3-one and Beckmann rearrangement of its oxime were studied.
Russian Journal of Organic Chemistry published new progress about Baeyer-Villiger oxidation. 1885-29-6 belongs to class nitriles-buliding-blocks, name is 2-Aminobenzonitrile(Flakes or Chunks), and the molecular formula is C7H6N2, Category: nitriles-buliding-blocks.
Referemce:
Nitrile – Wikipedia,
Nitriles – Chemistry LibreTexts