• Source: 2-Hydroxy-5-methoxybenzaldehyde

5.180.24.3/info/2" target="_blank">2-5.180.24.3/info/hydroxy" target="_blank">Hydroxy-5-methoxybenzaldehyde is an organic compound and an isomer of vanillin.




Synthesis and reactions


The chemical is produced by the Reimer-Tiemann reaction on 4-methoxyphenol with a 79% yield.
It reacts with malononitrile to form 5.180.24.3/info/2" target="_blank">2-imino-6-methoxy-2H-1-benzopyran-3-carbonitrile. It can be reduced by sodium borohydride in ethanol to form 5.180.24.3/info/2" target="_blank">2-5.180.24.3/info/hydroxy" target="_blank">hydroxy-5-methoxybenzyl alcohol.




See also


Vanillin
Isovanillin
ortho-Vanillin
5.180.24.3/info/2" target="_blank">2-5.180.24.3/info/hydroxy" target="_blank">Hydroxy-4-methoxybenzaldehyde




References

Kata Kunci Pencarian:

• 2-Hydroxy-5-methoxybenzaldehyde
• Vanillin
• Isovanillin
• 2-Hydroxy-4-methoxybenzaldehyde
• Ortho-Vanillin
• C8H8O3
• Mequinol
• List of additives in cigarettes
• Aldol condensation
• Vanilla