( E )-1-(5-methyl-1-(4-nitrophenyl)-1 H -1,2,3-triazol-4-yl)-3-(naphthalen-2-yl)prop-2-en-1-one

Kariuki, Benson M. ORCID: https://orcid.org/0000-0002-8658-3897, Abdel-Wahab, Bakr F., Mohamed, Hanan A. and El-Hiti, Gamal A. ORCID: https://orcid.org/0000-0001-6675-3126 2022. ( E )-1-(5-methyl-1-(4-nitrophenyl)-1 H -1,2,3-triazol-4-yl)-3-(naphthalen-2-yl)prop-2-en-1-one. Molbank 2022 (4) , M1464. 10.3390/m1464

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Abstract

A reaction of equimolar equivalents of 2-naphthaldehyde (1) and 1-(5-methyl-1-(4-nitrophenyl)-1H-1,2,3-triazol-4-yl)ethan-1-one (2) in ethanolic sodium hydroxide at 20 °C for 4 h gave (E)-1-(5-methyl-1-(4-nitrophenyl)-1H-1,2,3-triazol-4-yl)-3-(naphthalen-2-yl)prop-2-en-1-one (3) in 92% yield. Nuclear magnetic resonance spectroscopy and single-crystal X-ray diffraction were used to establish the structure of 3.

Item Type:	Article
Date Type:	Published Online
Status:	Published
Schools:	Schools > Chemistry
Additional Information:	License information from Publisher: LICENSE 1: URL: https://creativecommons.org/licenses/by/4.0/, Type: open-access
Publisher:	MDPI
Date of First Compliant Deposit:	17 November 2022
Date of Acceptance:	10 October 2022
Last Modified:	13 May 2023 17:16
URI:	https://orca.cardiff.ac.uk/id/eprint/154276

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