Economic, One-Pot Synthesis of Diethyl Furoxan Dicarboxylate

被引:0
作者
Thoenen, Michael [1 ,2 ]
Scherschel, Nicholas F. [1 ,2 ]
Piercey, Davin G. [1 ,2 ,3 ]
机构
[1] Purdue Univ, Sch Mat Sci & Engn, W Lafayette, IN 47907 USA
[2] Purdue Univ, Purdue Energet Res Ctr, W Lafayette, IN 47906 USA
[3] Purdue Univ, Sch Mech Engn, W Lafayette, IN 47906 USA
关键词
nitrile oxide; diethyl furoxan-3; 4-dicarboxylate; esters; energetic materials; NITRILE OXIDE CYCLOADDITIONS; ISOXAZOLINES; DERIVATIVES;
D O I
10.1021/acs.oprd.4c00191
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Diethyl furoxan dicarboxylate (DFD) is a starting material for fields as diverse as drug discovery, energetics, and any application where a furoxan or furazan may be desired. As with many disubstituted furoxans, they are synthesized via the dimerization of the appropriate nitrile oxide. Past procedures to form DFD involve low-yield destructive nitrations, multiple steps, halogenated solvents, or heavy or precious metals. Although these methods are functional enough for lab-scale preparations of DFD, they do not hold up well for economical scale-up. Our reported procedure improves the synthesis of DFD such that it is available from economical and commercially available starting materials in a single-step, one-pot, high-yield (98.5%) synthesis of material with a trivial workup in high purity (98.2% by H-1 quantitative NMR against a 2,4,6-trimethoxy-1,3,5-triazene standard). This improved procedure requires no organic solvents or heavy metals and is the most scalable preparation for this material to date.
引用
收藏
页码:3808 / 3812
页数:5
相关论文
共 28 条
[1]  
BARDOS TJ, 1966, TETRAHEDRON LETT, P1759
[2]  
Bouveault M. M., 1902, SOC CHIM FR, V27, P1164
[3]   Synthesis of 3-Aryl/benzyl-4,5,6,6a-tetrahydro-3aH-pyrrolo[3,4-d]isoxazole Derivatives: A Comparison between Conventional, Microwave-Assisted and Flow-Based Methodologies [J].
Castellano, Sabrina ;
Tamborini, Lucia ;
Viviano, Monica ;
Pinto, Andrea ;
Sbardella, Gianluca ;
Conti, Paola .
JOURNAL OF ORGANIC CHEMISTRY, 2010, 75 (21) :7439-7442
[4]   Nitrile oxide cycloadditions to olefinated sugars [J].
Colinas, PA ;
Jäger, V ;
Lieberknecht, A ;
Bravo, RD .
TETRAHEDRON LETTERS, 2003, 44 (05) :1071-1074
[5]   1,3-cycloaddition of nitrile oxides in ionic liquids. An easier route to 3-carboxy isoxazolines, potential constrained glutamic acid analogues [J].
Conti, D ;
Rodriquez, M ;
Sega, A ;
Taddei, M .
TETRAHEDRON LETTERS, 2003, 44 (28) :5327-5330
[6]   Nitroacetonitrile as a versatile precursor in energetic materials synthesis [J].
Creegan, Shannon E. ;
Piercey, Davin G. .
RSC ADVANCES, 2020, 10 (65) :39478-39484
[7]   NITROSATION OF PRIMARY ALIPHATIC DIAZOCARBONYL COMPOUNDS - FORMATION OF ALPHA-CARBONYL NITRILE OXIDES [J].
DAHN, H ;
FAVRE, B ;
LERESCHE, JP .
HELVETICA CHIMICA ACTA, 1973, 56 (01) :457-460
[8]   THE FUROXAN SYSTEM AS A USEFUL TOOL FOR BALANCING HYBRIDS WITH MIXED ALPHA(1)-ANTAGONIST AND NO-LIKE VASODILATOR ACTIVITIES [J].
FRUTTERO, R ;
BOSCHI, D ;
DISTILO, A ;
GASCO, A .
JOURNAL OF MEDICINAL CHEMISTRY, 1995, 38 (25) :4944-4949
[9]   STEREOSELECTIVE CYCLOADDITION OF NITRILE OXIDES TO A DISPIROKETAL-PROTECTED BUT-3-ENE-1,2-DIOL [J].
GRAVESTOCK, MB ;
PATON, RM ;
TODD, CJ .
TETRAHEDRON-ASYMMETRY, 1995, 6 (11) :2723-2730
[10]  
HIRAI K, 1972, CHEM PHARM BULL, V20, P97