Preliminary research toward the total synthesis of a novel crown ether that is a potential fluorescent chemosensor for potassium ion recognition
The purpose of this research was to synthesize a novel crown ether compound that has been designed to fluoresce with greatly enhanced intensities when in the presence of selected alkali metal cations. The novel crown ether compound (cryptand) 12,25-(1,5 - dimethyloxynaphtho)-1,4,7,10,14,17,20,23-oct...
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ndltd-BSU-oai-cardinalscholar.bsu.edu-handle-1854042014-08-07T03:32:40ZPreliminary research toward the total synthesis of a novel crown ether that is a potential fluorescent chemosensor for potassium ion recognitionShi, DanxinCrown ethers.Ions -- Spectra.The purpose of this research was to synthesize a novel crown ether compound that has been designed to fluoresce with greatly enhanced intensities when in the presence of selected alkali metal cations. The novel crown ether compound (cryptand) 12,25-(1,5 - dimethyloxynaphtho)-1,4,7,10,14,17,20,23-octaoxacyclohexacosane (1) was synthesized through 6 steps. The general synthetic route for the preparation of cryptand 1 is given in the proposed synthetic procedure. Reaction of benzaldehyde (23) with glycerol (24) in the presence of concentrated sulfuric acid afforded cis and traps-1,3-O-benzylideneglycerol (25). Cis and trans-2-O-benzyl-1,3-O-benzylideneglycerol (27) was obtained when 1,3O-benzylideneglycerol (25) was treated with benzyl bromide (26) and sodium wire in benzene. Acid-hydrolysis of the 2-O-benzyl-1,3-O-benzylideneglycerol (27) in methanol gave 2-O-benzylglcerol (28). The key starting material is 12,25-bisbenzyloxy1,4,7,10,14,17,20,23-octaoxacyclohexacosane (31), which requires the formation of four carbon-oxygen bonds. 2-O-benzylglcerol (28) was reacted with triethyene glycol ditosylate and sodium hydride in dioxane. This treatment gave the product 12,25-bisbenzyloxy1,4,7,10,14,17,20,23-octaoxacyclohexacosane likely to be (31) along with the 1:1 and a 3:3 crown ether products. The compound likely to be (31) was treated with H2 and a Pd/Ccatalyst and the resulting compound was 12,25-dihydroxy-1,4,7,10,14,17,20,23Octaoxacyclohexacosane (2). Compound likely to be (2) was reacted with 1,5bis(bromomethy)naphthalene and potassium t-butoxide in tetrahydrofuran to give the final cryptand compound 1. The structures of the crown ethers, the products of this reaction, have not yet been unambiguously assigned.Department of ChemistryBall State University. Dept. of Chemistry.Sousa, Lynn R.2011-06-03T19:37:14Z2011-06-03T19:37:14Z19951995xii, 91 leaves : ill. ; 28 cm.LD2489.Z78 1995 .S45http://cardinalscholar.bsu.edu/handle/handle/185404http://liblink.bsu.edu/uhtbin/catkey/941374Virtual Press |
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Crown ethers. Ions -- Spectra. |
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Crown ethers. Ions -- Spectra. Shi, Danxin Preliminary research toward the total synthesis of a novel crown ether that is a potential fluorescent chemosensor for potassium ion recognition |
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The purpose of this research was to synthesize a novel crown ether compound that has been designed to fluoresce with greatly enhanced intensities when in the presence of selected alkali metal cations. The novel crown ether compound (cryptand) 12,25-(1,5 - dimethyloxynaphtho)-1,4,7,10,14,17,20,23-octaoxacyclohexacosane (1) was synthesized through 6 steps. The general synthetic route for the preparation of cryptand 1 is given in the proposed synthetic procedure. Reaction of benzaldehyde (23) with glycerol (24) in the presence of concentrated sulfuric acid afforded cis and traps-1,3-O-benzylideneglycerol (25). Cis and trans-2-O-benzyl-1,3-O-benzylideneglycerol (27) was obtained when 1,3O-benzylideneglycerol (25) was treated with benzyl bromide (26) and sodium wire in benzene. Acid-hydrolysis of the 2-O-benzyl-1,3-O-benzylideneglycerol (27) in methanol gave 2-O-benzylglcerol (28). The key starting material is 12,25-bisbenzyloxy1,4,7,10,14,17,20,23-octaoxacyclohexacosane (31), which requires the formation of four carbon-oxygen bonds. 2-O-benzylglcerol (28) was reacted with triethyene glycol ditosylate and sodium hydride in dioxane. This treatment gave the product 12,25-bisbenzyloxy1,4,7,10,14,17,20,23-octaoxacyclohexacosane likely to be (31) along with the 1:1 and a 3:3 crown ether products. The compound likely to be (31) was treated with H2 and a Pd/Ccatalyst and the resulting compound was 12,25-dihydroxy-1,4,7,10,14,17,20,23Octaoxacyclohexacosane (2). Compound likely to be (2) was reacted with 1,5bis(bromomethy)naphthalene and potassium t-butoxide in tetrahydrofuran to give the final cryptand compound 1. The structures of the crown ethers, the products of this reaction, have not yet been unambiguously assigned. === Department of Chemistry |
author2 |
Ball State University. Dept. of Chemistry. |
author_facet |
Ball State University. Dept. of Chemistry. Shi, Danxin |
author |
Shi, Danxin |
author_sort |
Shi, Danxin |
title |
Preliminary research toward the total synthesis of a novel crown ether that is a potential fluorescent chemosensor for potassium ion recognition |
title_short |
Preliminary research toward the total synthesis of a novel crown ether that is a potential fluorescent chemosensor for potassium ion recognition |
title_full |
Preliminary research toward the total synthesis of a novel crown ether that is a potential fluorescent chemosensor for potassium ion recognition |
title_fullStr |
Preliminary research toward the total synthesis of a novel crown ether that is a potential fluorescent chemosensor for potassium ion recognition |
title_full_unstemmed |
Preliminary research toward the total synthesis of a novel crown ether that is a potential fluorescent chemosensor for potassium ion recognition |
title_sort |
preliminary research toward the total synthesis of a novel crown ether that is a potential fluorescent chemosensor for potassium ion recognition |
publishDate |
2011 |
url |
http://cardinalscholar.bsu.edu/handle/handle/185404 http://liblink.bsu.edu/uhtbin/catkey/941374 |
work_keys_str_mv |
AT shidanxin preliminaryresearchtowardthetotalsynthesisofanovelcrownetherthatisapotentialfluorescentchemosensorforpotassiumionrecognition |
_version_ |
1716710138506641408 |