Pyrolytic study of 3,4-Dimethyl-thiophene-2,5-dicarbonyl dichloride. Study of syntheis of a-oxo-para-quinodimethane
碩士 === 國立中山大學 === 化學研究所 === 86 === This thesis includes two parts. In the first part, we studied the pyrolytic chemistry of 3,4-Dimethyl-thiophene-2,5-dicarbonyl dichloride(67) . We used bromine as the trapping agent and obtained bromobenzene(73), p-bromochlorobenzene(74), p-dibromobenz...
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ndltd-TW-086NSYSU0650022016-06-29T04:13:29Z http://ndltd.ncl.edu.tw/handle/71136900395346703833 Pyrolytic study of 3,4-Dimethyl-thiophene-2,5-dicarbonyl dichloride. Study of syntheis of a-oxo-para-quinodimethane 3,4-二甲基-2,5-二氯化羰基吩之熱解化學α-氧代-對-二甲之合成研究 Wu Hui-Lan 吳蕙蘭 碩士 國立中山大學 化學研究所 86 This thesis includes two parts. In the first part, we studied the pyrolytic chemistry of 3,4-Dimethyl-thiophene-2,5-dicarbonyl dichloride(67) . We used bromine as the trapping agent and obtained bromobenzene(73), p-bromochlorobenzene(74), p-dibromobenzene(75), and compounds with molecular formulas C5H5ClBr2(76) and C5H4Br4(77) as the main products.In the second part, FVP of 4-methyl benzoyl chloride(42) was performed. When methanol was used as a trapping agent, FVP of 42 gave methyl 4-methylbenzoate(45) as only product. When compound 42 was photolyzed in furan with l=254nm, 3-(4-methylbenzoyl)furan(46) and 2-(4-methylbenzoyl)furan(47) were obtained as the major products. Chou Chin-Hsing 周金興 1998 學位論文 ; thesis 0 zh-TW |
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碩士 === 國立中山大學 === 化學研究所 === 86 === This thesis includes two parts. In the first part, we studied the pyrolytic chemistry of 3,4-Dimethyl-thiophene-2,5-dicarbonyl dichloride(67) . We used bromine as the trapping agent and obtained bromobenzene(73), p-bromochlorobenzene(74), p-dibromobenzene(75), and compounds with molecular formulas C5H5ClBr2(76) and C5H4Br4(77) as the main products.In the second part, FVP of 4-methyl benzoyl chloride(42) was performed. When methanol was used as a trapping agent, FVP of 42 gave methyl 4-methylbenzoate(45) as only product. When compound 42 was photolyzed in furan with l=254nm, 3-(4-methylbenzoyl)furan(46) and 2-(4-methylbenzoyl)furan(47) were obtained as the major products.
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author2 |
Chou Chin-Hsing |
author_facet |
Chou Chin-Hsing Wu Hui-Lan 吳蕙蘭 |
author |
Wu Hui-Lan 吳蕙蘭 |
spellingShingle |
Wu Hui-Lan 吳蕙蘭 Pyrolytic study of 3,4-Dimethyl-thiophene-2,5-dicarbonyl dichloride. Study of syntheis of a-oxo-para-quinodimethane |
author_sort |
Wu Hui-Lan |
title |
Pyrolytic study of 3,4-Dimethyl-thiophene-2,5-dicarbonyl dichloride. Study of syntheis of a-oxo-para-quinodimethane |
title_short |
Pyrolytic study of 3,4-Dimethyl-thiophene-2,5-dicarbonyl dichloride. Study of syntheis of a-oxo-para-quinodimethane |
title_full |
Pyrolytic study of 3,4-Dimethyl-thiophene-2,5-dicarbonyl dichloride. Study of syntheis of a-oxo-para-quinodimethane |
title_fullStr |
Pyrolytic study of 3,4-Dimethyl-thiophene-2,5-dicarbonyl dichloride. Study of syntheis of a-oxo-para-quinodimethane |
title_full_unstemmed |
Pyrolytic study of 3,4-Dimethyl-thiophene-2,5-dicarbonyl dichloride. Study of syntheis of a-oxo-para-quinodimethane |
title_sort |
pyrolytic study of 3,4-dimethyl-thiophene-2,5-dicarbonyl dichloride. study of syntheis of a-oxo-para-quinodimethane |
publishDate |
1998 |
url |
http://ndltd.ncl.edu.tw/handle/71136900395346703833 |
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