Mal, Kajal; Mukhopadhyay, Chhanda published the artcile< Chromatography free expeditious green synthesis of 3-hydroxy-2-pyrrolidone derivatives under eco-friendly conditions via the oxidation of benzyl amines without catalyst>, Product Details of C7H8BrN, the main research area is hydroxypyrrolidone preparation green chem; benzyl amine dialkylacetylenedicarboxylate oxidation.
A sustainable and atom economic one-pot synthesis of biol. significant 3-hydroxy-2-pyrrolidone moieties via the reaction of benzyl amine, aniline (or another benzyl amine) and dialkylacetylenedicarboxylate without catalyst in green solvent has been developed. Some remarkable features of this green procedure are aqueous ethanol solvent, reaction without catalyst, no column chromatog. for isolation of the products, higher the value of atom economy (AE) (up to 94.30%) and lower the E-factor value (up to 0.23 g/g). The reaction principally demonstrates the scope of oxidation of benzyl amines followed by cyclization. This synthetic route is also applicable to gram-scale synthesis.
Journal of Molecular Structure published new progress about Aromatic amines Role: RCT (Reactant), RACT (Reactant or Reagent). 3959-07-7 belongs to class bromides-buliding-blocks, and the molecular formula is C7H8BrN, Product Details of C7H8BrN.
Referemce:
Bromide – Wikipedia,
bromide – Wiktionary