Welcome to Open Science
Contact Us
Home Books Journals Submission Open Science Join Us News
Synthesis and Reactivity of Tetrakis Oxirane (Ylmehtyl) BisPhenyl Carbonodihydrazide (TOY-BPCH) Compound
Current Issue
Volume 4, 2017
Issue 3 (June)
Pages: 18-25   |   Vol. 4, No. 3, June 2017   |   Follow on         
Paper in PDF Downloads: 36   Since Nov. 23, 2017 Views: 1106   Since Nov. 23, 2017
Authors
[1]
Muhammad Rizwan, Department of Chemistry, University of Engineering & Technology, Lahore, Pakistan.
[2]
Sobia Naseem, Department of Chemistry, University of Engineering & Technology, Lahore, Pakistan.
Abstract
Catalyst Free based synthesis of Tetrakis Oxirane (Ylmehtyl) BisPhenyl Carbonodihydrazide with Multi- reactive group of Epoxides has been developed based on a sharpless Sym. Diphenylcarbazide in combination of hot Ethanol and Epichlorohydrin. A three component cycloaddition of a 1, 5 diphenyl carbazide, hot ethanol and epichlorohydrin to form a highly functionalized Tetrakis hydroxy chloro diphenyl carbazide (THCDPC) serves as the foundation for the synthesis of Tetrakis Oxiranes (ylmethyl) bisphenyl carbonodihydrazide (TOY-BPCH). The resulting product is followed by the neutralization with NaOH. Employing this approach the hydrophobic neutral based multi-reactive group of oxiranes bisphenyl carbonodihydrazide was synthesized in two steps and shown it 80% yield. The structure of the newly synthesized compound was characterized on the basis of FTIR, ¹H-NMR and LC-MS spectral data.
Keywords
1, 5-diphenylcarbazide, Epichlorohydrin, Hot Ethanol, Sod Hydroxide
Reference
[1]
Guangzeng L, S. Chen, Hong Fang M & Xiuyu L; J. Serb. Chem. 2007, 72, 475-484.
[2]
S. H Sanad; A, A Ismail; A, A Elmeligi; Electrochem. 1995, 11, 462.
[3]
A, A Ismaiel; S. H Sanad; A, A Elmeligi; Electrochem. 1994, 10, 448.
[4]
Ritu Jain; Veena Ch & A. K. Narula; Applied Polymer Science; 2007, 4, 2593-2598.
[5]
Pooja, S; Parveen. K; Veena Ch; AK Narula; IJEM Chem. 2005, 12, 259-264.
[6]
Lee, H; NEVILLE, K; Handbook of Epoxy resin.(MC Graw Hill, New York); 1972.
[7]
Van. N. Reinhold, Handbook of Composites. Edited by Lubin G (NY); 1982.
[8]
Iko K; Nakamura. Y; Yamaguchiand M; Imamura N; IEEE Elee Insul Mgg; 1990, 6, 25.
[9]
Hagiwara S; Ichimura S; Plastics. 1990, 39, 104.
[10]
Jain P; Ch. V; Varma IK; J Macromol Sci. Polym. Rev. 2002, C42, 139.
[11]
R. J Heath; Y. Di; S. Clara; A. Hudson; H. Manoch; Epoxide Tannage. 2005, 89 (5), 186-193.
[12]
Potter. W. G; Epoxide Resins, the Plastics Institute, London, 1970.
[13]
Ellis. B; Chemistry & Technology of Epoxy resins, Chapman & Hall Glasgow, 1993.
[14]
Oldring, P; Waterborne & Solvent based epoxies, Sita Technology Ltd, London, 1996.
[15]
Xing Hong Zhang; Yu Qin Min; Hui Zhao; Hong Mei Wan & Guo Rong Qi; Applied Polymer Science; 2006, 100, 3483-3489.
[16]
Courses. Washington.edu/medch402/Ch 2 Case Answer Online Version.
[17]
P. Sharma; V. Ch; A. K. Narula; Thermal Analysis & Calorimetry; 2008, 94, 805-815.
[18]
Siva Sankar Nayak; Ashoke Kumar Ghosh; Bikash Debnath; Satya Prakash Vishnoi & Tarun Jha; Ethnopharmacology; 2004, 93, 397-402.
Open Science Scholarly Journals
Open Science is a peer-reviewed platform, the journals of which cover a wide range of academic disciplines and serve the world's research and scholarly communities. Upon acceptance, Open Science Journals will be immediately and permanently free for everyone to read and download.
CONTACT US
Office Address:
228 Park Ave., S#45956, New York, NY 10003
Phone: +(001)(347)535 0661
E-mail:
LET'S GET IN TOUCH
Name
E-mail
Subject
Message
SEND MASSAGE
Copyright © 2013-, Open Science Publishers - All Rights Reserved