N-Methylimidazole-mediated synthesis of aryl alkyl ethers under microwave irradiation and solvent free conditions

被引:3
作者
Djahaniani, Hoorieh [1 ]
Aghadadashi-Abhari, Laila [2 ]
Mohtat, Bita [3 ]
机构
[1] Islamic Azad Univ, Dept Chem, East Tehran Branch, Tehran, Iran
[2] Payame Noor Univ, East Tehran Branch, Dept Chem, Tehran, Iran
[3] Islamic Azad Univ, Karaj Branch, Dept Chem, Karaj, Iran
关键词
microwave-assisted; three-component reaction; N-methylimidazole; O-alkylation; dialkyl acetylenedicarboxylate; O-ALKYLATION; PHENOL DERIVATIVES; ACETYLENEDICARBOXYLATES; 1-AZABUTA-1,3-DIENES; METHYLATION; ISOCYANIDES; ACYLATION;
D O I
10.2298/JSC131223027D
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A microwave-assisted three-component reaction was established for the synthesis of aryl alkyl ethers. The reaction was performed under solvent-free conditions in the presence of N-methylimidazole and dialkyl acetylenedicarboxylate to furnish a novel approach to O-alkylation of phenol derivatives in high yield.
引用
收藏
页码:459 / 464
页数:6
相关论文
共 17 条
[1]  
[Anonymous], BULL ENVIRON PHARMAC
[2]   Vapour phase O-methylation of 2-naphthol over the solid bases alkali-loaded silica and Cs-loaded MCM-41 [J].
Bal, R ;
Chaudhari, K ;
Sivasanker, S .
CATALYSIS LETTERS, 2000, 70 (1-2) :75-78
[3]   O-Alkylation of phenol derivatives via a nucleophilic substitution [J].
Cazorla, Clement ;
Pfordt, Emilie ;
Duclos, Marie-Christine ;
Metay, Estelle ;
Lemaire, Marc .
GREEN CHEMISTRY, 2011, 13 (09) :2482-2488
[4]   Balancing acidity and basicity for highly selective and stable modified MgO catalysts in the alkylation of phenol with methanol [J].
Choi, WC ;
Kim, JS ;
Lee, TH ;
Woo, SI .
CATALYSIS TODAY, 2000, 63 (2-4) :229-236
[5]   Reaction of phthalhydrazide and acetylenedicarboxylates in the presence of N-heterocycles: an efficient synthesis of phthalazine derivatives [J].
Ghahremanzadeh, Ramin ;
Ahadi, Somayyeh ;
Sayyafi, Maryam ;
Bazgir, Ayoob .
TETRAHEDRON LETTERS, 2008, 49 (29-30) :4479-4482
[6]   Selective alkylation of phenol with tert-butyl alcohol catalyzed by Bronsted acidic imidazolium salts [J].
Gui, JZ ;
Ban, HY ;
Cong, XH ;
Zhang, XT ;
Hu, ZD ;
Sun, ZL .
JOURNAL OF MOLECULAR CATALYSIS A-CHEMICAL, 2005, 225 (01) :27-31
[7]   A comparison of several modern alkylating agents [J].
Lamoureux, Guy ;
Agueero, Christian .
ARKIVOC, 2009, :251-264
[8]  
Lee S. W., 1997, HWAHAK KONGHAK, V35, P621
[9]   O-alkylation of phenol derivatives over basic zeolites [J].
Lee, SC ;
Lee, SW ;
Kim, KS ;
Lee, TJ ;
Kim, DH ;
Kim, JC .
CATALYSIS TODAY, 1998, 44 (1-4) :253-258
[10]   Ionic liquids as reagent and reaction medium: Preparation of alkyl aryl ethers [J].
Mohanazadeh, Farajollah ;
Aghvami, Majid .
MONATSHEFTE FUR CHEMIE, 2007, 138 (01) :47-49