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3,5-二羟基联苄的合成方法改进

Synthesis of 3,5-dihydroxy-bibenzyl
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摘要 目的改进3,5-二羟基联苄的合成方法。方法以3,5-二甲氧基苯甲醛为起始原料,经过Wittig反应、还原反应、脱甲基反应共3步反应得到目标化合物。结果成功地合成了3,5-二羟基联苄,总收率为88.2%。结论改进后的合成方法反应时间明显缩短,操作方法大大简化,收率由40%提高到88.2%。 Aim To improve the synthetic procedure of 3, 5-dihydroxy-bibenzyl. Methods 3, 5-dihydroxy-bibenzyl was prepared in 3 steps from starting material 3, 5-dimethoxybenzaldehyde, followed by Wittig reaction, reduction and demethylation. Results The target compound was provided in a total yield of 88.2%. Conclusion Compared with other reported methods, the operation was simplified, the reaction time was shortened and the yield was raised from 40% to 88.2%.
出处 《中国药物化学杂志》 CAS CSCD 2008年第2期129-130,134,共3页 Chinese Journal of Medicinal Chemistry
关键词 化学合成 3 5-二羟基联苄 联苄大麻素 chemical synthesis 3, 5-dihydroxy-bibenzyl bibenzyl cannabinoid
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  • 1DUNCAN R, ALISON J, DRYSDALE R G, et al. Differential effects of cannabis extracts and pure plant cannabinoidson hippocampal neurones and glia [ J ]. Neurosci Lett, 2006, 408(3) : 236 - 241.
  • 2BUDNEY A J, Vandrey R G, Hughes J R, et al. Oral delta-9-tetrahydrocannabinol suppresses cannabis with drawal symptoms [J]. Drug Alcohol Depend, 2007, 86 (1):22-29.
  • 3WILKINSON J D, WILLIAMSON E M. Cannabinoids inhibit human keratinocyte proliferation through a non-CB1/CB2 mechanism and have a potential therapeutic value in the treatment of psoriasis[J] .J Dermatol Sci, 2007, 45(2) :87 - 92.
  • 4TOYOTA M, KINUGAWA T, ASAKAWA Y. Bibenzyl cannabinoid and bisbibenzyl derivative from the liverwort radula perrottetii [J]. Phytochemistry, 1994, 37(3) :859 - 862.
  • 5TOYOTA M, SHIMAMURA T, ISHII H, et al. New bibenzyl cannabinoid from the New Zealand Liverwor-tradula marginata [J]. Chem Pharm Bull, 2002, 50 (10) : 1390 - 1392.
  • 6LESLIE W, CROMBIE W, MARY L, et al. Synthesis of bibenzyl cannabinoids, hybrids of two biogenetic series found in Cannabis sativa [J]. J Chem Soc.. Perkin Trans I, 1988(5) : 1263 - 1270.
  • 7ALI M A, KONDO K, TSUDA Y. Synthesis and nematocidal activity of hydroxystilbenes[J]. Chem Pharm Bull, 1992, 40(5) : 1130 - 1136.

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