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594306435

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x分别与α-萘酚和β-萘酚发生威廉姆逊反应生成醚, 然后醚上的酯基在KOH碱性条件下水解, 两步反应“一锅法”完成, 使合成化合物3a, 3b 的产率分别由两步法的43.8%和63.9%提高到“一锅法”的85.1%和91.2%, 方法简便, 易处理.
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way2009way6860

金虫 (正式写手)


594306435(金币+1, 翻译EPI+1): 谢谢 2011-03-11 13:15:47
引用回帖:
Originally posted by 594306435 at 2011-03-11 11:02:08:
x分别与α-萘酚和β-萘酚发生威廉姆逊反应生成醚, 然后醚上的酯基在KOH碱性条件下水解, 两步反应“一锅法”完成, 使合成化合物3a, 3b 的产率分别由两步法的43.8%和63.9%提高到“一锅法”的85.1%和91.2%, 方法简便 ...

x react with α-naphthol and β-naphthol to ether respectively by Williamson reaction, then ester on the ether hydrolysis in the condition of alkaline KOH . The "one pot" method complete the two-step reaction, and the yield of product compounds 3a, 3b were 85.1% and 91.2%, which is better than  the yield of 43.8% and 63.9% through  two-step method. In the whole, the one pot method is simple and easy to handle.
2楼2011-03-11 11:32:52
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shuaishuai90

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594306435(金币+2): 感谢 2011-03-11 13:15:58
The ether is formed by the Williamson reaction of X with Alpha alpha-naphthol and Beta alpha-naphthol dividedly, then estergroup on the ethers will be hydrolyzed under the koh alkaline condition
3楼2011-03-11 11:34:54
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way2009way6860

金虫 (正式写手)


594306435(金币+2): 谢谢这么严谨的对待我的求助 再次表示感谢 2011-03-11 13:16:37
修改后:x react with α-naphthol and β-naphthol to ether respectively by Williamson reaction, then ester on the ether hydrolysis in the condition of alkaline KOH . The "one pot" method complete the two-step reaction, and the yield of product compounds 3a, 3b were 85.1% and 91.2%, which is better than  the corresponding yield of 43.8% and 63.9% through  two-step method. In the whole, the one pot method is simple and easy to handle.
4楼2011-03-11 11:35:38
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