期刊文献+

4-(二苯氨基)苯甲醛的合成工艺改进

Process Improvement on the Synthesis of 4-( Diphenylamino) benzaldehyde
下载PDF
导出
摘要 以Al Cl3为催化剂,三苯氨(1)和原甲酸三乙酯(2)为原料,合成了4-(二苯氨基)苯甲醛(3),其结构经1H NMR和FT-IR确证。合成3的较佳工艺条件为:1 40 mmol,n(1)∶n(2)∶n(Al Cl3)=1∶5∶8,苯为溶剂,于30℃反应4 h,收率91%。 4-(Diphenylamino) benzaldehyde (3) was synthesized by the reaction of triphenylamine (1) with triethyl orthoformate (2) using aluminium trichloride as the catalyst. The structure was con- firmed by 1H NMR and FT-IR. The optimum reaction conditions of synthesizing 3 at 30 ℃ for 4 h were as follows: 1 was 40 retool, n(1) :n(2) :n(A1CI3) = 1:5:8, benzene was solvent. The yield was 91% under the optimum reaction conditions.
出处 《合成化学》 CAS CSCD 2015年第3期249-251,共3页 Chinese Journal of Synthetic Chemistry
基金 国家自然科学基金资助项目(21103151) 浙江省重点科技创新团队资助项目(2010R50018)
关键词 原甲酸三乙酯 4-(二苯氨基)苯甲醛 合成 工艺改进 triethyl orthoformate 4-(diphenylamino) benzaldehyde synthesis process improvement
  • 相关文献

参考文献19

  • 1Xia C Y, Wang X M, Lin J, eta/. Organic light-emitting devices(OLED) based on new triphenylamine derivatives [J]. Synthetic MetaLs ,2009,159(3 -4) :194 -200.
  • 2Wang D Q, Qin C X, Wang X M, et al. Synthesis of branched chromophores with enhanced two-photon ab- sorption via coreeffect [ J ]. Optical Materials ,2009,31 : 805 -811.
  • 3Hua J L, Li B, Meng F S, et al. Two-photon absorp- tion propertie of byperbranched conjugated polymers with triphenylamine as the core [ J ]. Polymer, 2004,45 : 7143 -7149.
  • 4Jeong S, Kim M K, Kim S H, et al. Effcient deep - blue emitters based on triphenylamine-linked benzimid- azole derivatives for nondoped fuorescent organic light- emitting diodes [ J ]. Organic Electronics, 2013, 14 (10) :2497 -25o4.
  • 5Lee K H, Kim C S, Kim Y K, eta/. t-Butyl group- substituted triphenylamine-containing orange-red fuo- re.scent emitters for organic light-emitting diodes [ J ]. Thin Solid Films,2012,520 ( 11 ) :3946 - 3951.
  • 6Tarsanga R, Promarakb V, Sudyoadauka T, et al. Tuning the electron donating ability in the triphenyl- amine-based D - "tr - A architecture for highly efficient dye-sensitized solar cells [ J ]. Journal of Photochemistry and Photobiology A: Chemistry,2014,273 : 8 - 16.
  • 7Liu X S, Cao Z C, Huang H L, et al. Novel D -D -'u- A organic dyes based on triphenylamine and indole-deriv- atives for high performance dye-sensitized solar cells[ J]. Journal d Power Sources,2014,248:400-406.
  • 8Zou Y P, Sang G Y, Wu W P, et aL A polythiophene derivative with octyloxyl triphenylamine-vinylene onju- gated side chain:Synthesis and its applications in reid- effect transistor and polymer solar cell [ J ]. Synthetic Metals,2009,159(3 -4) :182 - 187.
  • 9James S Swensen, Wang L, James E. Rainbolt,character- ization of solution processed,p-doped films using hole-on- ly devices and organic field-effect transistors[ J ]. Materi- als Research Society ,2012,13(12) :3085 - 3090.
  • 10Tian H N, Yang X C, Chen R K, et al. Effect d dif-ferent dye baths and dye-structures on the perform- ance of dye-sensitized solar cells based on triphenyl- amine dyes [ J ]. Journal of Physical Chemistry C, 2008,11(29) :11023 - 11033.

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部