59259-45-9

Upstream product

• 62055-72-5 N'-(2,4-dinitrophenyl)-N'-methylbenzohydrazide 
• 98-88-4 benzoyl chloride 
• 19255-35-7 1-methyl-1-(2,4-dinitrophenyl)hydrazine 

Downstream Products

• 62055-72-5 N'-(2,4-dinitrophenyl)-N'-methylbenzohydrazide 
• 90913-90-9 Z-N-(2,4-dinitrophenyl)-N-methylbenzenecarbohydrazonoyl 4-nitrobenzenethiolate 
• 62055-89-4 C₁₅H₁₄N₄O₅ 
• 62055-86-1 C₁₅H₁₄N₄O₅ 
• 134917-93-4 ethyl (Z)-N-(2,4-dinitrophenyl)-N-metyhylbenzohydrazonate 

Relevant academic research and scientific papers

Kinetic and Stereochemical Study on Bimolecular Substitution Reactions of Hydrazonates, Thiohydrazonates, and Hydrazonoyl Chlorides with Methoxide Ion

Reaction of the (Z)-hydrazonoyl chlorides 2 with methoxide ion in methanol, under conditions where kinetic results show the reaction is bimolecular, leads to stereospecific formation of the (Z)-methyl hydrazonates 5.Less than 2percent of the product with the "inverted" configuration at carbon (6) is formed.When a poorer leaving group than Cl(-) is involved, then mixtures of E and Z products result.Thus the aryl thiohydrazonates (3) which have the Z configuration give 84-90percent of the (Z)-methyl hydrazonate on reaction with methoxide ion.The (E)-aryl hydrazonates undergo reaction ca. 12-fold more slowly and isomer ratios of the (Z)- and (E)-methyl hydrazonates which result are closer to 1:1.The product methyl hydrazonates 5 and 6 undergo MeO(-)-catalysed interconversion to an equilibrium mixture which favors 6, but at a slower rate than the formation of either 5 or 6.The stereochemical outcome of these displacements at the C=N bond is rationalized in terms of stereoelectronic control of the addition and elimination steps.