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紫檀茋的制备 被引量:3

Synthesis of Pterostilbene
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摘要 3,5-二甲氧基氯苄与对苄氧基苯甲醛经格氏反应、固体酸催化剂NaHSO4·SiO2催化脱水制得中间体(E)-3,5-二甲氧基-4'-苄氧基二苯乙烯,再经Pd/Al-MCM-41介孔分子筛催化氢化脱苄制得紫檀茋,总收率为77%。 Pterostilbene was synthesized from 3,5-dimethoxy benzyl chloride and 4-benzyloxybenzaldehyde by Grignard reaction, catalytic dehydration with solid acid NaHSO4"SiO2 to obtain the intermediate (E)-3,5-dimethoxy-4'- benzyloxystilbene, followed by debenzylation in the presence of hydrogen and mesoporous molecular sieve Pd-grafted A1-MCM-41 with the overall yield of about 77 %.
出处 《中国医药工业杂志》 CAS CSCD 北大核心 2014年第9期816-817,839,共3页 Chinese Journal of Pharmaceuticals
基金 浙江省重点科技创新团队项目(2010R50017)
关键词 紫檀茋 3 5-二甲氧基苄氯 格氏反应 NaHSO4 SIO2 AL-MCM-41 合成 pterostilbene 3,5-dimethoxy benzyl chloride Grignard reaction NaHSO4·SiO2 A1-MCM-41 synthesis
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参考文献12

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共引文献13

同被引文献41

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