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1,8-二甲氧基乙基萘的合成 被引量:1

Synthesis of 1,8-Bis(2-methoxylethyl)-naphthalene
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摘要 以1,8-二萘酸酐为原料,经氢化铝锂还原得1,8-二羟甲基萘(2);2经浓盐酸酸化生成1,8-二氯甲基萘(3);3经氢化铝锂还原为1,8-二甲基萘(4);用强碱丁基锂和叔丁醇钾将4转化成二钾盐后与甲氧基氯甲烷反应合成了1,8-二甲氧基乙基萘,其结构经1HNMR和13C NMR和HR-MS表征。 Naphthalic anhydride was reduced to 1,8-bis (hydroxylmethyl) -naphthalene (2) by lithium aluminum hydride, then was treated by concentrated hydrochloric to form 1,8-bis (chloromethyl)naphthalene (3). 3 was reduced to 1,8-dimethylnaphthalene (4) by lithium aluminum hydride again. 4 was transferred to the dipotassium salt of 4 and then directly reaction with chloro(methyl) methane to gain 1,8-bis (2-methoxylethyl) -naphthalene (5). The structures were characterized by 1H NMR, 13C NMR and HR-MS.
出处 《合成化学》 CAS CSCD 北大核心 2009年第5期634-636,共3页 Chinese Journal of Synthetic Chemistry
关键词 1 8-二羟甲基萘 1 8-二氯甲基萘 1 8-二甲基萘 1 8-二甲氧基乙基萘 合成 1,8-bis ( hydroxylmethyl ) naphthalene 1,8-bis ( chloromethyl ) naphthalene 1,8-dimethylnaphthalene 1,8-bis(2-methoxylethyl)-naphthalene synthesis
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  • 66: ^1H NMR δ: 1.54(m, 3H, CH3), 3.35(s, 3H, OCH3), 3.43(s, 3H, OCH3), 3.60-3.67(m, 2H, CH2), 3.72-3.76(m, 2H, CH2), 5.28 5.34(m, 1H, CH), 7.36 -7.88(m, 6H, Phil).
  • 7^13C NMR δ: 25.24, 37.78, 56.40, 58.78, 74.60, 76.45, 124.20, 124.76, 125.27, 129.15, 129.42, 130.54, 130.69, 133.62, 135.67, 140.95.

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