73315-72-7

Upstream product

• 2666-86-6 4-methyl-N-(5-nitro-furan-2-ylmethylene)-aniline 
• 106-49-0 p-toluidine 
• 20782-91-6 2-(bromomethyl)-5-nitrofuran 

Downstream Products

• 116507-18-7 Allyl-(5-nitro-furan-2-ylmethyl)-p-tolyl-amine 
• 175603-41-5 ((E)-But-2-enyl)-(5-nitro-furan-2-ylmethyl)-p-tolyl-amine 
• 116531-14-7 7-Nitro-3-p-tolyl-10-oxa-3-aza-tricyclo[5.2.1.0^1,5]dec-8-ene 

Relevant academic research and scientific papers

New substituted alkenyl-furfuryl-aryl amines: Synthesis and their characterization

Reaction of several N-(5-substituted-2-furfuryl)-p-toluidines with the appropriate substituted allyl bromide gave new examples of tertiary amines (3a-e, 4a-e) with unique capability to react spontaneously in a sense of intramolecular [4+2]cycloaddition (I

Studies in the Furan Series. 23. Preparation of some New 5-Substituted furfurylallylarylamines. Influence of Substituents on the Intramolecular Diels-Alder (IMDA) Reaction

Several new N-allyl-N-(5-substituted)-2-furfuryl-p-toluidines IIIa-e with Cl, Br, I, NO2 or CH3O groups in position 5 of the furan nucleus were prepared by allylation of the corresponding secondary furfurylarylamines.Both, electron withdrawing and releasi

ALIPHATIC AND AROMATIC 5-NITRO-2-FURYLAMINES AND AROMATIC 5-NITROFURFURYL ETHERS

Tertiary 5-nitrofurylamines were prepared by a nucleophilic substitution of 5-nitro-2-furfuryl bromide (I) with aliphatic secondary amines.According to reaction conditions N-(5-nitro-2-furfuryl)-X-phenylamines or their mixture with N,N-di(5-nitro-2-furfuryl)-X-phenylamines were obtained from the reaction of I with substituted primary aromatic amines.Compound I gave with 2-aminophenol a mixture of O- and N-mono- and disubstituted derivatives, and with ethyl salicylate ethyl 2-(5-nitro-2-furfuryloxy)benzoate.