2-Hydroxy-3-octyloxybenzaldehyde

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-res...

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Bibliographic Details
Published in:MolBank 2021-09, Vol.2021 (3), p.M1264
Main Authors: Novoselova, Julia V., Vereshchagin, Anatoliy A., Kalnin, Arseniy Y., Lukyanov, Daniil A., Levin, Oleg V.
Format: Article
Language:English
Subjects:
2-hydroxy-3-octylbenzaldehyde
Alkylation
Cardiovascular disease
Chromatography
Conflicts of interest
Coordination compounds
Energy storage
Fourier transforms
Ligands
Mass spectrometry
NMR
Nuclear magnetic resonance
Phase transitions
Research parks
SalEn precursor
Schiff base
Transition metals
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Summary: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).
ISSN:1422-8599
1422-8599
DOI:10.3390/M1264