Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Water | HCID 962 | — |
| Edukt | N-bromobutanimide | HCID 67184 | — |
| Edukt | 4,4'-Didodecyl-2,2'-bithiophene | HCID 21917265 | — |
| Lösungsmittel | Acetic acid chloroform | HCID 21584526 | — |
| Produkt | 5-Bromo-4,4'-didodecyl-2,2'-bithiophene | HCID 67120820 | 85% |
Reaktionsschritte
To a solution of 4,4′-didodecyl-2,2′-bithiophene (0.100 g, 0.199 mmol) in CHCl3/HOAc (1:1) (Vt=2.0 mL) at 0° C. was added N-bromosuccimide (NBS, 35.7 mg, 0.199 mmol) in portions over a period of 45 minutes. The reaction mixture was stirred for 1 hour at 0° C. and overnight at room temperature. The reaction mixture was poured into water (50.0 mL) and extracted with chloroform (3×50.0 mL). The combined organic phases were washed with water (50.0 mL), NaOH solution, and dried over MgSO4. After filtration through Celite, the filtrate was concentrated in vacuo and the residue was purified by column chromatography on silica gel (hexanes) to provide 5-bromo-4,4′-didodecyl-2,2′-bithiophene (29A) as a colorless oil (98.0 mg, 85% yield). 1H NMR (CDCl3): δ 0.84-1.54 (m, 46H), 2.57 (m, 4H), 6.81 (s, 1H), 6.84 (s, 1H), 6.94 (s, 1H).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | USRE044304E1 |
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| Quelldatensatz | uspto-grants-2013_06 |
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| ORD ID | ord-76cd16eac47841e4bc50a1a442274da4 |
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| Quellennotiz | uspto-grants-2013_06 |
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