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3,6-二氨基-N-异丁基邻苯二甲酰亚胺的合成 被引量:2

Synthesis of 3,6-Diamino-N-isobutyl Phthalimide
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摘要 以3-硝基邻苯二甲酸为原料,经脱水成酐、氨解、还原酰化、硝化、水解、还原等六步反应合成了一种新型的环芳酰胺的构筑单元对苯二胺衍生物——3,6-二氨基-N-异丁基邻苯二甲酰亚胺,总收率16.4%,其结构经1H NMR,13C NMR和ESI-MS表征。 A novel derivative of phenylene diamine,3,6-diamino-N-isobutyl phthalimide,was designed and synthesized by a six-step reaction of dehydration,ammonolysis,reduction and acylation,nitration,hydrolysis and hydrogenation from 3-nitrophthalic acid.The total yield was 16.4% and the structures were characterized by 1H NMR,13C NMR and ESI-MS.
出处 《合成化学》 CAS CSCD 北大核心 2011年第6期744-746,共3页 Chinese Journal of Synthetic Chemistry
关键词 3 6-二氨基-N-异丁基邻苯二甲酰亚胺 3-硝基邻苯二甲酸 对苯二胺衍生物 合成 3 6-diamino-N-isobutylphthalimide 3-nitrophthalic acid p-phenylene diamine derivative synthesis
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参考文献18

  • 1胡晋川,冯文,李向晖,杨柳青,袁立华,何兰,龚兵.芳酰胺类大环一步高效合成及其成环机理研究进展[J].物理化学学报,2010,26(7):1811-1822. 被引量:4
  • 2钟凯,朱槿,邓金根.折叠物的超分子行为研究进展[J].合成化学,2007,15(6):667-676. 被引量:1
  • 3Yuan L H, Feng W, Yamato K, et al. Highly effi- cient, one-step macrocyclizations assisted by the folding and preorganization of precursor oligomers [ J ]. J Am Chem Soc,2004,126 : 11120 - 11121.
  • 4Feng W, Yamato K, Yang L Q, et al. Efficient kinet- ic macrocyclization [ J ]. J Am Chem Soc, 2009,131 : 2629 - 2637.
  • 5Zou S L, He Y Z, Yang Y A, et 02. Improving the ef- ficiency of forming ' Unfavorable' products : Eight-resi-due macrocycles from folded aromatic oligoamide pre- cursors [ J ]. Synlett,2009,9 : 1437 - 1440.
  • 6Yang L Q, Zhong L J, Yamato K, et al. Aromatic oli- goamide macrocycles from the bimolecular coupling of folded oligomeric precursors [ J ]. New J Chem, 2009, 33:729 - 733.
  • 7Yuan L H, Sanford A R, Feng W, et al. Synthesis of crescent aromatic oligoamides [ J ]. J Org Chem, 2005, 70 : 10660 - 10669.
  • 8Zhang Y F, Yamato K, Zhong K, et al. Aggregation and columnar assembly of crescent olig0amides [ J ]. Org Lett ,2008,10:4339 - 4342.
  • 9张云峰,钟凯,朱槿,邓金根.芳香寡聚酰胺类化合物的合成[J].合成化学,2009,17(5):574-576. 被引量:1
  • 10杨永安,袁立华,胡晋川,邹树良,冯文,龚兵.带极性侧链的环[6]芳酰胺的球形自组装[J].物理化学学报,2010,26(6):1557-1564. 被引量:6

二级参考文献244

  • 1程晓红,鞠秀萍,HOEGER,Sigurd.官能团化刚性大环的超分子化学[J].有机化学,2006,26(5):733-743. 被引量:9
  • 2Gellman S H, Foldamers. A manifesto[J]. Ace Chem Res, 1998,31 : 173 - 180.
  • 3Hill D J, Mio M J, Moore J S, et al. A field guide to foldamers [ J ]. Chem Rev,2001,101 : 3893 - 4011.
  • 4Zhu J, Parra R D, Zeng H Q, et al. A new class of folding oligomers: cresent oligoamides[ J]. J Am Chem Soc,2000,122 : 4219 - 4220.
  • 5Gong B, Zeng H Q, Zhu J, et al. Creating nanocavities of tunable sizes:Hollow helices[J]. Pro Nad Acad Sci USA ,2002,99 : 11583 - 11588.
  • 6Yuan L H, Zeng H Q, Gong B, et al. Helical aromatic oligoamides: Reliable, readily predictable folding from the combination of rigidified structural motifs[ J]. J Am Chem Soc,2004,126:6528 -16537.
  • 7Zhang Y F, Zhu J, Deng J G, et al. Aggregation and columnar assembly of crescent oligoamides [ J ]. Org Lett ,2008,10:4339 - 4342.
  • 8Yuan L H, Sanford A R, Gong B, et al. Synthesis of crescent aromatic oligoamides [ J ]. J Org Chem,2005, 70 : 10660 - 10669.
  • 91c: ^1H NMR δ: 10.13(s, 1H), 10.00(s, 1H), 9.64 (s, 1H), 9.29(s, 1H), 8.98(s, 1H), 8.72(s, 1H), 8.63(dd, J= 1.5 Hz, 7.5 Hz, 1H ), 7.02 - 6.97(m, 2H), 6.87(dd, J=1.4 Hz, 7.6 Hz, 1H ), 6.52(s, 1H), 6.50(s, 1H), 6.18(s, 1H), 4.47(t, J=4.8 Hz, 2H), 4.28 -4.26(m, 4H), 4. 07(brs, 4H), 3.97-3.94(m, 2H), 3.92 -3.88(m, 11H), 3.77 -3.47(m, 30H), 3.44 -3.43(m, 4H), 3.33 (s, 3H), 3.30(s, 6H), 3.28(s, 3H).
  • 10^13C NMR6: 162.6, 161.8, 160.8, 159.7, 156.0, 154.2, 152.8, 152.3, 151.1, 148.2, 132.4, 130.5, 128.7, 123.9,123.0, 122.9, 122.9, 121.2, 120.8, 120.4, 114.5, 114.3, 113.1, 109.8, 98.9, 97.5, 94.1, 71.7, 71.6, 70.8, 70.5, 70.3, 70.3, 70.2, 70.2, 70.2, 69.6, 69.3, 69.1, 69.0, 68.8, 68.7, 68.4, 58.7, 58.6, 55.8, 55.8, 55.5.

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