2-Hydroxy-3-octyloxybenzaldehyde

Julia V. Novoselova; Anatoliy A. Vereshchagin; Arseniy Y. Kalnin; Daniil A. Lukyanov; Oleg V. Levin

doi:10.3390/M1264

Molbank (Aug 2021)

2-Hydroxy-3-octyloxybenzaldehyde

Julia V. Novoselova,
Anatoliy A. Vereshchagin,
Arseniy Y. Kalnin,
Daniil A. Lukyanov,
Oleg V. Levin

Affiliations

Julia V. Novoselova: Institute of Chemistry, St. Petersburg State University, Universitetskii pr. 26, Peterhof, 198504 St. Petersburg, Russia
Anatoliy A. Vereshchagin: Institute of Chemistry, St. Petersburg State University, Universitetskii pr. 26, Peterhof, 198504 St. Petersburg, Russia
Arseniy Y. Kalnin: Institute of Chemistry, St. Petersburg State University, Universitetskii pr. 26, Peterhof, 198504 St. Petersburg, Russia
Daniil A. Lukyanov: Institute of Chemistry, St. Petersburg State University, Universitetskii pr. 26, Peterhof, 198504 St. Petersburg, Russia
Oleg V. Levin: Institute of Chemistry, St. Petersburg State University, Universitetskii pr. 26, Peterhof, 198504 St. Petersburg, Russia

DOI: https://doi.org/10.3390/M1264
Journal volume & issue: Vol. 2021, no. 3
p. M1264

Abstract

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Herein, we report the chromatography-free synthesis of 2-hydroxy-3-octyloxybenzaldehyde by the alkylation of 2,3-dihydroxybenzaldehyde as a promising precursor for new SalEn-type complexes with transition metals. The structure of the product is elucidated by means of 1H and 13C-NMR spectra, high-resolution mass spectrometry with electrospray ionization (ESI-HRMS) and Fourier-transform infrared spectroscopy (FTIR).

Published in Molbank

ISSN: 1422-8599 (Online)
Publisher: MDPI AG
Country of publisher: Switzerland
LCC subjects: Science: Chemistry: Inorganic chemistry
Website: https://www.mdpi.com/journal/molbank

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