Oxidation of Thiols Using K2S2O8 in Ionic Liquid

被引:14
作者
Hajipour, Abdol R. [1 ,2 ]
Mostafavi, Majid [2 ]
Ruoho, Arnold E. [1 ]
机构
[1] Univ Wisconsin, Sch Med, Dept Pharmacol, Madison, WI 53706 USA
[2] Isfahan Univ Technol, Coll Chem, Pharmaceut Res Lab, Esfahan, Iran
基金
美国国家卫生研究院;
关键词
Disulfides; ionic liquid; K2S2O8; oxidation; thiols; NITROGEN DOUBLE-BONDS; BENZYLTRIPHENYLPHOSPHONIUM DICHROMATE; EFFICIENT OXIDANT; MILD REAGENT; CLEAVAGE; DEPROTECTION;
D O I
10.1080/10426500802417000
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
A green, straightforward, and novel method for oxidation of thiols to the corresponding disulfides is reported using K2S2O8 in the ionic liquid 1-butyl-3-methylimidazolium bromide [(bmim)Br] at 65-70 degrees C. The corresponding disulfides were obtained in excellent yield and short reaction time.
引用
收藏
页码:1920 / 1923
页数:4
相关论文
共 23 条
[1]  
BLOCK E, 1974, J AM CHEM SOC, V96, P1135
[2]   Novel bronsted acidic ionic liquids and their use as dual solvent-catalysts [J].
Cole, AC ;
Jensen, JL ;
Ntai, I ;
Tran, KLT ;
Weaver, KJ ;
Forbes, DC ;
Davis, JH .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2002, 124 (21) :5962-5963
[3]   Asymmetric interaction between rod cyclic GMP phosphodiesterase γ subunits and αβ subunits [J].
Guo, LW ;
Grant, JE ;
Hajipour, AR ;
Muradov, H ;
Arbabian, M ;
Artemyev, NO ;
Ruoho, AE .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (13) :12585-12592
[4]  
Hajipour A, 1999, INDIAN J CHEM B, V38, P461
[5]   Deprotection of thioacetals using K2S2O8/[bmim]Br as a mild and efficient reagent under solvent-free conditions [J].
Hajipour, Abdol R. ;
Mostafavi, Majid ;
Ruoho, Arnold E. .
MONATSHEFTE FUR CHEMIE, 2007, 138 (06) :569-572
[6]   Oxidative deprotection of trimethylsilyl ethers under solvent-free conditions using K2S2O8 in the presence of catalytic amount of [bmim]Br [J].
Hajipour, Abdol Reza ;
Mostafavi, Majid ;
Ruoho, Arnold E. .
CATALYSIS COMMUNICATIONS, 2007, 8 (11) :1825-1828
[7]   Methyltriphenylphosphonium peroxydisulfate and iodine as mild reagents for the iodination of activated aromatic compounds [J].
Hajipour, AR ;
Ruoho, AE .
ORGANIC PREPARATIONS AND PROCEDURES INTERNATIONAL, 2005, 37 (03) :279-283
[8]  
Hajipour AR, 2000, J CHEM RES, P32
[9]   Bis(1-benzyl-4-aza-1-azoniabicyclo[2.2.2]octane) peroxodisulfate: A mild and efficient oxidant for cleavage of nitrogen double bonds and oxidation of alcohols under anhydrous conditions [J].
Hajipour, AR ;
Mohammadpoor-Baltork, I ;
Kianfar, G .
BULLETIN OF THE CHEMICAL SOCIETY OF JAPAN, 1998, 71 (11) :2655-2659
[10]   Wet silica-supported permanganate for the cleavage of semicarbazones and phenylhydrazones under solvent-free conditions [J].
Hajipour, AR ;
Adibi, H ;
Ruoho, AE .
JOURNAL OF ORGANIC CHEMISTRY, 2003, 68 (11) :4553-4555