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Use of NMR and Mass Spectrometry in Establishing the Structures of Ring Opening products of 3- Methyl- 4,1- Benzoxazepine-2,5- Dione in Acid and Basic Media

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dc.contributor.author SAMINA ALAM
dc.contributor.author ZAHEER-UD-DIN BABER
dc.contributor.author KHAN, NAEEMA
dc.date.accessioned 2023-08-25T10:11:43Z
dc.date.available 2023-08-25T10:11:43Z
dc.date.issued 2000-12-03
dc.identifier.citation Alam, S., Baber, Z. U. D., & Khan, N. (2000). Use of NMR and mass spectrometry in establishing the structures of ring opening products of 3-methyl-4, 1-benzoxazepine-2, 5-dione in acid and basic media. JOURNAL OF THE CHEMICAL SOCIETY OF PAKISTAN, 22(4), 299-302. en_US
dc.identifier.issn 0253-5106
dc.identifier.uri http://142.54.178.187:9060/xmlui/handle/123456789/19561
dc.description.abstract 3-Methyl-4,1-benzoxazepine-2.5-dione (I) when stirred for lr hours in methanolic solution with a few drops of 10 %. NaOH below 60 degreesC gave solid crystalline product (m.p. 100-102 degreesC, 51% yield). H-1 NMR and MS analysis confirmed structure (II) which suggest the cleavage of C-O bond but when (I) was treated with a few drops of 10% HCl under similar temperature yielded compound (III) as a liquid which gave evidence for C-N bond cleavage giving no traces of the former product (II). en_US
dc.description.sponsorship The chemical society of Pakistan is an approved society from the PSF en_US
dc.language.iso en en_US
dc.publisher Karachi: International Centre for Chemical and Biological Sciences, H.E.J. Research Institute of Chemistry, University of Karachi en_US
dc.title Use of NMR and Mass Spectrometry in Establishing the Structures of Ring Opening products of 3- Methyl- 4,1- Benzoxazepine-2,5- Dione in Acid and Basic Media en_US
dc.type Article en_US


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