28163-00-0Relevant articles and documents
Direct oxidative conversion of benzylhalides, -amines, -alcohols, and arylaldehydes to nitriles with trans-3,5-dihydroperoxy-3,5-dimethyl-1,2-dioxolane activated by NH4Br
Azarifar, Davood,Najminejad, Zohreh
, p. 107 - 111 (2015/01/30)
A simple and efficient oxidative conversion of benzyl derivatives of halides, amines, alcohols, and aldehydes into corresponding nitriles is described using trans-3,5-dihydroperoxy-3,5-dimethyl-1,2-dioxolane in the presence of NH4Br. The reactions proceeded smoothly at room temperature to afford the products in high-to-excellent yields. Graphical Abstract: [Figure not available: see fulltext.]
Synthesis of aryl nitriles using the stable aryl diazonium silica sulfates
Habibi, Davood,Heydari, Somayyeh,Nasrollahzadeh, Mahmoud
, p. 573 - 574,2 (2020/09/16)
An efficient method for preparation of aryl nitriles is reported using Cu(I) to catalyse the reaction of aryl diazonium silica sulfates with sodium cyanide under mild conditions at room temperature in water. This method has the advantages of high yields,
3-Chloro-4-cyanophenyl 4'-substituted benzoates
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, (2008/06/13)
Disclosed are compounds of the formula: STR1 wherein R is an alkyl group having 1 to 8 carbon atoms and X is a dioxane, cyclohexane, or benzene ring. The compounds of the invention are suitable as liquid crystal materials in electrooptical displays. Specifically, when added to nematic liquid crystals, these compounds provide an increase in the positive dielectric anisotropy of the liquid crystal composition.