CAS: 4542-77-2; 2,6-Bis(Bromomethyl)Naphthalene

该化合物是一种溴化芳香化合物,在环角的2和6个位置上有两个活性溴甲基组,这一结构使该化合物成为有机合成中有价值的中间体,特别是交叉反应和聚合化学.其高活性使得能够高效地发挥作用,便利了复杂的分子结构的构建.该化合物通常用于制备先进材料,包括液晶和凝聚聚合物,因为其硬性丙烯基质.在受控制的条件下,其定义明确的再活性和稳定性使制药,农用化学品和材料科学方面的研究人员有一个可靠的选择.适当的处理由于其对湿度和光度的敏感度而至关重要.

结构式图片

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上下游产品

2.6-dimethylnaphthalene naphthalene-2,6-dimethanol dimethyl 2,6-naphthalenedicarboxylate 2,6-Bis-acetoxymethyl-naphthalin 2,6-naphthalenedicarbaldehyde cis,cis-2.6-Bis(p-methylstyryl)naphthalen cis,trans-2.6-Bis(p-methylstyryl)naphthalen

合成工艺路线路线简述

  • 合成目标产物 2 6-Bis(Bromomethyl)Naphthalene 97 主要起始原料 Dimethyl 2,6-Naphthalenedicarboxylate
  • (文献来源)合成步骤主要原料 Dimethyl 2,6-Naphthalenedicarboxylate
📜2,6-二甲基萘置于n-溴代丁二酰亚胺(Nbs),偶氮二异丁腈体系中,用 四氯化碳 作为反应溶剂,化学反应生成 2,6-双(溴甲基)萘
参考文献:Molecular Recognition In Ternary Complexes Ofγ-Cyclodextrin With Naphthalenedicarboxylate Ions And A Space-Regulator Ion
标题:Molecular Recognition In Ternary Complexes Ofγ-Cyclodextrin With Naphthalenedicarboxylate Ions And A Space-Regulator Ion
摘要:在碱性d2O中,γ-环糊精(γ-Cd)与2,6-萘二甲酸根离子(2,6-Ndc)的络合反应在加入2,6-双(1-吡啶基甲基)萘二溴化物(2,6-Pmn)作为空间调节剂后得到了极大增强.通过1H NMR光谱法,结合诱导圆二色光谱和紫外吸收光谱的测量,证实了γ-Cd,2,6-Ndc和2,6-Pmn之间形成1:1:1的三元络合物.通过曲线拟合法分析了在过量2,6-Pmn和ndc区域异构体存在的情况下γ-Cd质子的化学位移(δ)变化,从而得到了ndc与γ-Cd-2,6-Pmn二元络合物的结合常数(k6).k6值按1,5-Ndc < 1,4-Ndc < 1,8-Ndc < 1,3-Ndc < 1,6-Ndc < 2,3-Ndc < 2,7-Ndc < 2,6-Ndc的顺序增加,表明γ-Cd与2,6-Pmn的二元络合物能够识别ndc的分子结构.γ-Cd空腔和2
DOI:10.1246/bcsj.71.2323

海关参考信息

专利信息


专利号:US-6495710-B2
优先权日:2000-01-14
标题:Synthesis and use of dimethyl 1,5-naphthalenedicarboxlyates and intermediates therefrom
发明人:MACEK JOHN A; ROSEN BRUCE I; HOLZHAUER JUERGEN K; BRAMLET JOHN S; LILLWITZ LARRY D; SCHNEIDER DAVID J; LANG LAWRENCE L; PASCHKE EDWARD E; WEIS JOHN M; VISWANATH YENAMANDRA; SAKELLARIDES STEFANOS L
权利人:BP CORP NORTH AMERICA INC
摘要:The synthesis of dimethyl-1,5-naphthalenedicarboxylate and polymers and articles formed therefrom is disclosed, as well as applications for dimethyl-1,5-naphthalenedicarboxylate, its corresponding acid 1,5-NDA, and various synthesis intermediates.

专利号:KR-20030044364-A
优先权日:2001-11-29
标 题 :Novel phase transfer catalyst and its application for the synthesis of α-amino acid

专利号:US-2001031852-A1
优先权日:2000-01-14
标 题 :Synthesis and use of dimethyl 1,5-naphthalenedicarboxylates and intermediates therefrom

专利号:EP-1368297-A2
优先权日:2000-01-14
标题:Synthesis and use of dimethyl-1,5-naphthalenedicarboxylates and intermediates therefrom

专利号:JP-2004501862-A
优先权日:2000-01-14
标题 :Synthesis and use of intermediates from dimethyl-1,5-naphthalenedicarboxylate and dimethyl 1,5-naphthalenedicarboxylate

专利号:MX-PA02006832-A
优先权日:2000-01-14
标 题:SYNTHESIS AND USE OF THE 1,5-NAFTALENODICARBOXILATOS DIMETILICOS AND ITS INTERMEDIARIES.

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合成参考文献


参考文献:10.1038/s44160-023-00340-4
摘要:Schmidt BVKJ. MOF-made polyacenes. Nat. Synth. 2023 Jun 16;2(9):813–4. doi: 10.1038/s44160-023-00340-4.
参考文献:10.1038/s44160-023-00310-w
摘要:Kitao T, Miura T, Nakayama R, Tsutsui Y, Chan YS, Hayashi H, Yamada H, Seki S, Hitosugi T, Uemura T. Synthesis of polyacene by using a metal–organic framework. Nat. Synth. 2023 May 04;2(9):848–54. doi: 10.1038/s44160-023-00310-w.
参考文献:10.1007/s11426-025-2668-9
摘要:Wu B, Tang R, Liu Y, Li Z, Lin F, Sun Z, Pi Y, Ouyang G, Tan Y. Efficient iodine adsorption from seawater by simple macrocycle and mechanistic insights. Sci. China Chem. 2025 Jun 24;68(10):4929–39. doi: 10.1007/s11426-025-2668-9.
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