Synthesis of 2-Hydroxy-5-methoxy-3-alkyl-1,4-benzoquinones
Corresponding Author(s) : LIQIANG WU
wliq1974@sohu.com
Asian Journal of Chemistry,
Vol. 21 No. 9 (2009): Vol 21 Issue 9
Abstract
A short, efficient synthesis of 2-hydroxy-5-methoxy-3-alkyl-1,4- benzoquinones is described. Ultrasound-assisted Wittig reaction of alkyltriphenyl phosphonium bromides with 2-hydroxy-3,6-dimethoxybenzaldehyde in basic aqueous condition followed by reduction with Na/n-BuOH gave 3,6-dimethoxy-2-alkylphenols. Oxidation of 3,6- dimethoxy-2-alkylphenols with Fremy's salt produced 2,5-dimethoxy- 3-alkyl-1,4-benzoquinones. Selective hydrolysis with perchloric acid converted 2,5-dimethoxy-3-alkyl-1,4-benzoquinones to 2-hydroxy-5- methoxy-3-alkyl-1,4-benzoquinones.
Keywords
Ultrasound irradiation
2-Hydroxy-5-methoxy-3-alkyl-1,4-benzoquinones
2-Hydroxy-3,6-dimethoxybenzaldehyde
Wittig reaction
WU, L., YANG, C., & YANG, L. (2010). Synthesis of 2-Hydroxy-5-methoxy-3-alkyl-1,4-benzoquinones. Asian Journal of Chemistry, 21(9), 7005–7011. Retrieved from https://asianpubs.org/index.php/ajchem/article/view/12177
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