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(¤@) Pyrolytic and photolytic studies of substituted styrylarenes (¤G) Pyrolytic studies of 2-inden-1-ylidenemethylthiophene and 2-inden-1-ylidenemethylfuran.

The first chapter describe the pyrolytic and photolytic studies of substituted styrylarenes. Flash vacuum pyrolysis (FVP) of (2-(4-methoxystyryl)-N-methylindole) (18) gave (4-vinylphenol) (81)¡B (7-methyl-7H-benzo[c]carbazole) (82)¡B (benzo[c]carbazole) (83)¡B (1,6-dihydrocyclopenta[c]carbazole) (84) and (3,6-dihydrocyclopenta- [c]carbazole) (84'). FVP of 2',3,5-trimethoxystilbene (31) gave 2-(3,5-dihydroxyphenyl)benzo[b]furan) (26) and 2-(3,5-dimethoxy- phenyl)benzo[b]furan (95). FVP of 2-methoxy-4-(methoxymethyl)-1- [2-(4-methoxyphenyl)-1-methylvinyl]benzene (33) gave [2-(4- methoxyphenyl)-3-methylbenzofuran-5-yl]methanol (104)¡B4-(3,5- dimethylbenzofuran-2-yl)phenol (105) and 2-(4-hydroxyphenyl)-3- methylbenzofuran-5-carbaldehyde (106). FVP of 2-(2-chlorostyryl)- benzo[b]furan (44) ¡B2-(2-chlorostyryl)benzo[b]thiophene (45) and 2-(2-chlorostyryl)-N-methylindole (46) gave benzo[b]naphtha[1,2-d]- furan (116)¡Bbenzo[b]naphtho[1,2-d]thiophene (117)¡B7-methyl-7H- benzo[c] carbazole (82) and benzo[c]carbazole (83). FVP of 2-chloro-N-(N-methylindol-2-ylmethylene)aniline (71) gave N-methylindole-2-carbonitrile (124)¡B 7H-indolo[2,3-c]quinoline (125) and indolo[1,2-a]quinoxaline (126). FVP of 2-methoxy -N-(N-methyl- indol-2-ylmethylene)aniline (72) gave N-methylindole-2-carbonitrile (124) ¡B 2-(N-methylindol- 2-yl)benzoxazole (132) and 2-hydroxy- benzonitrile (133). FVP of 2-methylthio-N-(phenylmethylene)aniline (73)¡B2-methylthio-N-(furylmethylene)aniline (74)¡B2-methylthio-N- (benzo[b]thiophen-2-ylmethylene)aniline (75) and 2-methylthio-N- (N-methylindol-2-ylmethylene)aniline (76) gave 2-phenylbenzothiazole (143)¡B2-furylbenzothiazole (144)¡B2-benzo[b]thiophen-2-ylbenzo- thiazole (145)¡B2-(N-methylindol-2-yl)benzothiazole (146)¡B2-(1H- indol-2-yl)benzothiazole (147) and benzothiazole (148).Such a method, via oxygen-carbon bond disconnecting, can synthesize efficiently a nature product, stemofuran A 26.
Photolytic study of 2',3,5-trimethoxystilbene (31) gave 1,5,7- trimethoxyphenanthrene) (101). Photolytic studies of 2-(2-chloro- styryl)benzo[b]furan (44) ¡B2-(2-chlorostyryl)benzo[b]thiophene (45) and 2-(2-chlorostyryl)-N-methylindole (46) gave benzo[b]naphtha- [1,2-d]furan (116) and 4-chlorobenzo[b]naphtha[1,2-d]furan (120)¡Bbenzo[b]naphtho[1,2-d]thiophene (117) and 4-chlorobenzo[b]naphtha- [1,2-d]thiophene (120) ¡B7-methyl-7H- benzo[c]carbazole (82) and 4-chloro-7-methyl-7H-benzo[c]carbazole (121). Photolytic studies of 2-methylthio-N-(phenylmethylene)aniline (73)¡B2-methylthio- -N-(furylmethylene)aniline (74)¡B2-methylthio-N-(benzo[b]thiophen-2- ylmethylene)aniline (75) and 2-methylthio-N-(N-methylindol-2- ylmethylene)aniline (76) gave 2-phenylbenzothiazole (143)¡B2-furyl- benzothiazole (144)¡B2-benzo[b]thiophen-2-ylbenzo- thiazole (145)¡B2-(N-methylindol-2-yl)benzothiazole (146)¡B2-(1H-indol-2-yl)benzo- thiazole (147) and 2-(2,4-dimethoxyphenyl)benzothiazole) (60f). Such a method has the potential for preparing drugs and application on material science.
(¤G)FVP of 2-inden-1-ylidenemethylthiophene (24) and 2-inden-1-ylidene- methylfuran (25) gave the cyclized products 2-(2'-thienyl)naphthalene (29) and 2-(2'-furyl)naphthalene (32).

Identiferoai:union.ndltd.org:NSYSU/oai:NSYSU:etd-1120107-105559
Date20 November 2007
CreatorsYu, Pin-Chih
ContributorsT.-Y. Dong, C. H. Chou, E.C. Wang, C.-C. Tzeng, Y.-H. Chu,
PublisherNSYSU
Source SetsNSYSU Electronic Thesis and Dissertation Archive
LanguageCholon
Detected LanguageEnglish
Typetext
Formatapplication/pdf
Sourcehttp://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-1120107-105559
Rightsnot_available, Copyright information available at source archive

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