• 대한화학회지
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• 제55권2호
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• pp.153-156
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• 2011

• Bulletin of the Korean Chemical Society
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• 제20권5호
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• pp.581-586
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• 1999

A series of polyethers containing the thiazole or oxazole subcyclic moiety have been synthesized. Reaction of 2-aryl-4-hydroxymethylthiazole with tetra- and pentaethylene glycol di-p-tosylate in THF provided corresponding α,ω-bis[2'-aryl-4'-methylthiazole]polyethylene glycol in good yields. Similar treatment of 2-phenyl-4-hydroxymethyloxazole 7 and 2-phenyl-5-hydroxymethyloxazole 8 with tetraethylene glycol di-p-tosylate yielded the corresponding 1,13-bis [2'-phenyl-4'-methyloxazole]tetraethylene glycol 16 and 1,13-bis[2'-phenyl-5'-methyloxazole]tetraethylene glycol 17 in 69 and 43% yields in respectively. The potentiometric properties of PVC-based ion selective membranes containing 66 wt% o-nitrophenyloctyl ether (NPOE) and 4 wt% polyethers 9-17 have been examined. The membranes containing thiazole and oxazole polyether derivatives exhibited high selectivity toward silver (I) ion. It was observed that the response slopes of the electrodes to silver ion vary with the length of polyether chain linking two thiazole subcyclic moiety. Potentiometric data suggest that the number of ether units, CH2OCH2, for phenylthiazole derivatives be greater than 5 to result in near-Nernstian response. However, the response behaviors of the membrane electrodes based on phenyloxazole podands 16 and 17, which have different orientation, were correspondingly similar to those of the electrodes based on phenylthiazole podands 9 and 10. On the other hand, the ISEs based on thiazole polyether derivatives with different terminal substituents, e.g., phenyl 10, naphtyl 14, and thienyl 15, except that with pyridyl 12, exhibited little difference in their potentiometric properties.

• 대한화학회지
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• 제36권3호
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• pp.453-459
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• 1992

염화 삼메틸규소를 첨가하지 않고 에테르나 사염화탄소 중의 3-Aryl-3-bromopropanoyl chloride를 상온에서 2당량의 히드록실아민과 반응시켜 2,5-diarylisoxazolidin-3-ones 을 좋은 수율로 얻을 수 있었다. 그러나 $0^{\circ}C$에서 3-bromohydrocinnamoyl chloride 는 2당량의 벤질히드록실아민과 반응하여 N-benzyl-3-bromo-3-phenylpropanohydroxamic acid (72%) 와 N-benzyl-C-phenylnitrone (12%)을 생성하며 같은 조건하에서 3당량의 벤질히드록실아민을 사용하면 3-phenylisoxazolidin-5-one (41%) 과 2-benzyl-S-phenyl-isoxzolidin-3-one (38%)이 생성된다.

• 대한화학회지
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• 제23권6호
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• pp.392-395
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• 1979

몇가지 유기할로겐화물, 즉 브롬화에틸, 염화부틸, 브롬화페닐 및 염화벤질등을 탄화수소중에서 그리냐르법으로 무수사염화주석과 반응시켰다. 이때 소량의 에테르를 그리냐르반응단계에서 계내에 투입하엿을 때 보다 용이하게 반응이 진행되어 좋은 수율로 유기주석화합물들을 얻을 수 있었다.