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...

Full description

Bibliographic Details
Main Authors: Wu Hui-Lan, 吳蕙蘭
Other Authors: Chou Chin-Hsing
Format: Others
Language:zh-TW
Published: 1998
Online Access:http://ndltd.ncl.edu.tw/handle/71136900395346703833
id ndltd-TW-086NSYSU065002
record_format oai_dc
spelling 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
collection NDLTD
language zh-TW
format Others
sources NDLTD
description 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.
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
work_keys_str_mv AT wuhuilan pyrolyticstudyof34dimethylthiophene25dicarbonyldichloridestudyofsyntheisofaoxoparaquinodimethane
AT wúhuìlán pyrolyticstudyof34dimethylthiophene25dicarbonyldichloridestudyofsyntheisofaoxoparaquinodimethane
AT wuhuilan 34èrjiǎjī25èrlǜhuàtāngjīfēnzhīrèjiěhuàxuéayǎngdàiduìèrjiǎzhīhéchéngyánjiū
AT wúhuìlán 34èrjiǎjī25èrlǜhuàtāngjīfēnzhīrèjiěhuàxuéayǎngdàiduìèrjiǎzhīhéchéngyánjiū
_version_ 1718325813772812288