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功能化离子液体[C_3SO_3Hnhm]HSO_4催化合成苯并氧杂蒽 被引量:1

Synthesis of benzoxanthene catalyzed by functionalized ionic liquids [C_3SO_3Hnhm] HSO_4
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摘要 无溶剂下以功能化酸性离子液体4-(3-磺丙基)吗啡啉硫酸氢盐([C_3SO_3Hnhm]HSO_4)为催化剂,催化β-萘酚和芳香醛合成苯并氧杂蒽。通过单因素试验和正交试验优化反应条件,并考察了该离子液体的重复使用性能。结果表明,当苯甲醛用量为0. 005 mol,β-萘酚与苯甲醛摩尔比为2∶1,催化剂用量为苯甲醛的6%,100℃下反应10 min后苯并氧杂蒽的产率达到91%以上。[C_3SO_3Hnhm]HSO_4催化剂重复使用5次,其催化活性下降不明显,为苯并氧杂蒽类化合物的绿色合成提供了一种新方法。 A solvent - free synthesis of benzoxanthene was operated, in which functionalized acidic ionic liquids, 4 - (3 - propanesulfonic acid) morphinehydrogen sulfate [ C3 SO3 Hnhm ] HSO4 were used as catalysts, and β-naphthol and aromatic aldehyde were used as raw materials. The reaction conditions were optimized by the single factor experiment and orthogonal experiment,and the reusability of the ionic liquid catalyst was also studied. The results show that when the dosage of benzaldehyde is 0.005 mol, the molar ratio of β - naphthol to benzaldehyde is 2:1, and the catalyst is in an amount corresponding to 6% of benzaldehyde, the yield can reach more than 91% after reaction for 10 min at 100℃. The catalytic activity of [ C3 SO3 Hnhm ] HSO4 was not significantly reduced for being reused 5 times. This work has provided a new method for green synthesis of benzoxanthene compounds.
作者 汤小芳 刘显明 周思言 李双 TANG Xiao-fang;LIU Xian-ming;ZHOU Si-yan;LI Shuang(Chemical Engineering Institute,Taizhou College of Science and Technology-,Nanjing University of Science and Technology,Taizhou,Jiangsu 225300,China)
出处 《日用化学工业》 CAS CSCD 北大核心 2018年第11期627-631,共5页 China Surfactant Detergent & Cosmetics
基金 江苏省高等学校大学生实践创新训练计划项目(2017025X)
关键词 功能化酸性离子液体 催化 苯并氧杂蒽 functionalized acidic ionic liquid catalyze benzoxanthene
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  • 1SYDNES L K, SANDBERG M. The reactivity of acylals towards gri- gnard and organolithium reagents [ J ]. Tetrahedron Lett, 1997,53 ( 37 ) : 12679 - 12690.
  • 2FREEMAN F, KARCHEFSKI E M. Preparation and spectral properties of benzylidene diacetates [ J ]. Chem Eng Data, 1977,22 ( 3 ) : 355 -357.
  • 3YADAV J S, REDDY B V S, SRINIVAS C. Indium trichloride cata- lyzed chemoselective conversion of aldehydes to gem -diacetates [ J ]. Synth Commun,2002,32 (5) :2149 - 2153.
  • 4SATYA V, RAJU N, SULFATED Z. An efficient catalyst for the sythe- sis of 1,1 - diacetates from aldehydes and ketones [ J ]. Chem Res, 1996,26(3) :68 -69.
  • 5BABAK K,HASSAN S,EBRAHIMIAN G R. Mild and efficient coner- sion of aldehydes to 1,1 - diacetates catalyzed with N - bromosucci- nimide (NBS) [ J]. Synlett,2000,22 ( 5 ) :623 - 624.
  • 6NABBJYOTI D, DIPOK J K, RULI B, et al. Locling as acetylation cata- lyst in the preparation of 1,1 - diacetates from aldehydes [ J ]. Org Chem, 1997,62 (3) : 1563 - 1564.
  • 7MAJID M H,HADIJED B,SHIMA T,et al. KHSO4 :A catalyst for the chem - selective preparation of 1,1 - diacetates from aldehydes under solvent - free conditions [ J ]. Green Chemistry, 2005,29 ( 7 ) : 867 - 869.
  • 8GUSTAVO P R, HORACIO J T, GRACIELA T B, et al. Solvent - free catalytic preparation of 1,1 - diacetates from aldehydes using a wells - dawson acid (H6P2W18 O62 · 24H2O) [J]. Tetrahedrom Letters, 2003,44( 1 ) :1301 - 1303.
  • 9WEITON T. Room - temperature ionic liquids solvent for synthesis and catalysis [ J ]. C hem Rev, 1999,99 ( 8 ) :2071 - 2803.
  • 10DUPONT J D, SOUZA R F, SUAREZ P A Z. Ionic liquid (molten salt) phase organometallic catalysis [ J ]. Chem Rev,2002,102 (10) : 3667 - 3692.

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