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Short Note

1-(4-Formyl-2,6-dimethoxyphenoxy)-4-chlorobut-2-yne

Institut Utinam UMR CNRS 6213, UFR Sciences et Techniques, Université de Bourgogne-Franche-Comté, 16 Route de Gray, 25030 Besançon, France
Academic Editor: Nicholas E. Leadbeater
Molbank 2021, 2021(3), M1252; https://doi.org/10.3390/M1252
Received: 21 June 2021 / Revised: 8 July 2021 / Accepted: 9 July 2021 / Published: 21 July 2021
(This article belongs to the Section Organic Synthesis)
A reaction of biomass-derived aldehyde synringaldehyde and half an equivalent of 1,4-dichlorobut-2-yne was attempted in order to obtain a bis-aldehyde with an alkyne spacer. The reaction was carried out in a basic media to effect bis O-alkylation, as described in literature for the preparation of structurally similar compounds. Nevertheless, only mono alkylation was observed. View Full-Text
Keywords: O-alkylation; Williamson reaction; ether derivatives; alkyne derivatives O-alkylation; Williamson reaction; ether derivatives; alkyne derivatives
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MDPI and ACS Style

Husson, J. 1-(4-Formyl-2,6-dimethoxyphenoxy)-4-chlorobut-2-yne. Molbank 2021, 2021, M1252. https://doi.org/10.3390/M1252

AMA Style

Husson J. 1-(4-Formyl-2,6-dimethoxyphenoxy)-4-chlorobut-2-yne. Molbank. 2021; 2021(3):M1252. https://doi.org/10.3390/M1252

Chicago/Turabian Style

Husson, Jérôme. 2021. "1-(4-Formyl-2,6-dimethoxyphenoxy)-4-chlorobut-2-yne" Molbank 2021, no. 3: M1252. https://doi.org/10.3390/M1252

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