1986
DOI: 10.1080/00397918608057741
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A Convenient Synthesis of 3-Alkylthiophenes

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Cited by 112 publications
(48 citation statements)
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“…3-hexylthiophene (3-HT) monomer was synthesized by coupling n-hexylmagnesium bromide with 3-bromothiophene in the presence of nickel catalyst [29]. P3HT was synthesized by a typical chemical oxidative in CHCl 3 .…”
Section: Synthesis and Preparationmentioning
confidence: 99%
“…3-hexylthiophene (3-HT) monomer was synthesized by coupling n-hexylmagnesium bromide with 3-bromothiophene in the presence of nickel catalyst [29]. P3HT was synthesized by a typical chemical oxidative in CHCl 3 .…”
Section: Synthesis and Preparationmentioning
confidence: 99%
“…Kumada coupling reaction 7,8 between 3-bromo thiophene and Grignard reagent of alkyl bromide resulted in 3-alkylthiophene 2 n , which was brominated with NBS, 9 and the obtained 2,5-dibromo-3-alkyl thiophene 3 n was coupled with 4-methoxyphenylboric acid 4 under a standard Suzuki condition. 10 Worth to be noted is that, the yield of Suzuki reaction between 2,5-dibromothiophene and 4-methoxyphenylboric acid was usually…”
Section: Resultsmentioning
confidence: 99%
“…2,5-Dibromo-3-alkylthiophene 3 n : All 2,5-dibromo-3-alkylthiophene derivatives were prepared according to a modified procedure of Zimmer et al 8 At 0-5 ℃ under an argon atmosphere, NBS powder (28 mmol) was added slowly to a stirred solution of 3-alkylthiophene (13.1 mmol) dissolved in a 1∶1 mixture of chloroform (15 mL) and DMF (15 mL). The mixture was stirred overnight at room temperature and then quenched with water, the organic layer was separated, and the water layer was extracted with chloroform (10 mL×3).…”
Section: -Alkylthiophenementioning
confidence: 99%
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“…Before the polymerization the initial monomer 3-hexylthiophene (3HT) must be activated to 2,5-dibromo-3-hexylthiophene [44][45][46]. 3HT is derived from 3-bromothiophene (a brominated thiophene) and bromohexane [47].…”
Section: Processing Of the Active Layermentioning
confidence: 99%