68095-64-7Relevant articles and documents
ELECTRON TRANSFER PROCESSES. REACTION OF 5-NITROFURYL DERIVATIVES GOING BY ANIONRADICAL MECHANISM
Prousek, Josef
, p. 3347 - 3353 (2007/10/02)
5-nitrofurfuryl nitrate and bromide (1a,b) react with electron donors to give 1,2-bis(5-nitro-2-furyl)ethane (II), 1,2-bis(5-nitro-2-furyl)ethylene (III), 5-nitro-2-methylfurane (IV), products of SRN1 reactions Va, Vb and other derivatives.Formation of the derivatives II to V is discussed on the basis of anionradical mechanism. 5-Nitrobenzyl bromide reacts by a SRN1 reaction with 5-nitrofurfuryl phenyl sulphone (Va) in basic medium to give 1-(5-nitro-2-furyl)-1-phenylsulphonyl-2-(4-nitrophenyl)ethane (VIII) and 1-(5-nitro-2-furyl)-2-(4-nitrophenyl)ethylene (IX).