Fang, Zhongxue published the artcileThe [4+1] cyclization reaction of 2-hydroxylimides and trimethylsulfoxonium iodide for the synthesis of 3-amino-2,3-dihydrobenzofurans, Product Details of C7H6N2, the main research area is amino dihydro benzofuran preparation green chem; hydroxylimide trimethylsulfoxonium iodide cyclization.
The [4+1] cyclization reaction of 2-hydroxylimides I (R1 = H, MeO, Cl; R2 = H, Br, Cl, NO2; R3= H; R2R3 = -CH=CH-CH=CH-; R4 = H, Me; R5 = 2,4,6-trimethylphenyl, quinolin-8-yl, pyrimidin-2-yl, etc.) and trimethylsulfoxonium iodide was investigated. This cyclization reaction exhibits wide scope and compatibility with functional groups. The 3-amino-2,3-dihydrobenzofurans II were obtained in reasonable to high yields under mild conditions. This methodol. was utilized to synthesize highly substituted 3-amino-2,3-dihydrobenzofuran derivatives II.
New Journal of Chemistry published new progress about Benzofurans Role: SPN (Synthetic Preparation), PREP (Preparation). 1885-29-6 belongs to class nitriles-buliding-blocks, name is 2-Aminobenzonitrile(Flakes or Chunks), and the molecular formula is C7H6N2, Product Details of C7H6N2.
Referemce:
Nitrile – Wikipedia,
Nitriles – Chemistry LibreTexts