A Comparative Study: Michael Adduct Reaction with Hydroxylamine Hydrochloride and Hydrazine Hydrate : Formation of Oximes, Indazolones, Hydrazides, 2-Mercaotp-1,3,4,-Oxadiazoles, Imonobenzal-N-Amides of Cyclohexanones and Study of Their Antimicrobial
Corresponding Author(s) : Anjali M. Rahatgaonkar
Asian Journal of Chemistry,
Vol. 11 No. 4 (1999): Vol 11 Issue 4
Abstract
A comparative study reveals that 1,2,4,5-tetrahydro-4-6-diaryl-in-dazoline-3-one-6-yl, 3,5-diaryl-6-carbohydrazide-2-ene-cyclo hexanone-3-yl and 3,5-diaryl-6-carbethoxy-2-ene cyclohexyl oxime were obtained by the reaction of 3,5-diaryl-6-carbathoxy-2-ene-cyclohexanone-3-yl with hydrazine hydrate and hydroxylamine hydrochloride in solvents S1, S2, S3 and S4 respectively. 3,5-Diaryl-6-carbohydrazide-2-ene-cyclohexanone-3-yl was further subjected to react with CS2/KOH and benzaldehydes to get 2-mercapto-1,3,4-oxadiazoles and Schiff bases respectively.
Keywords
Comparative Study
Michael Adduct Reaction
Hydroxylamine Hydrochloride
Hydrazine Hydrate
Formation
Oximes
Indazolones
Hydrazides
2-Mercaotp-1,3,4,-Oxadiazoles
Imonobenzal-N-Amides
Cyclohexanones
Study
Antimicrobial Activity
M. Rahatgaonkar, A. (2012). A Comparative Study: Michael Adduct Reaction with Hydroxylamine Hydrochloride and Hydrazine Hydrate : Formation of Oximes, Indazolones, Hydrazides, 2-Mercaotp-1,3,4,-Oxadiazoles, Imonobenzal-N-Amides of Cyclohexanones and Study of Their Antimicrobial . Asian Journal of Chemistry, 11(4), 1385–1390. Retrieved from https://asianpubs.org/index.php/ajchem/article/view/23499
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