Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1257980Erstellt: 27. Oktober 2026

Water → 5-Bromo-4,4'-didodecyl-2,2'-bithiophene

https://huagongshe.com/reaction/1257980

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktN-bromobutanimideHCID 67184—
Edukt4,4'-Didodecyl-2,2'-bithiopheneHCID 21917265—
LösungsmittelAcetic acid chloroformHCID 21584526—
Produkt5-Bromo-4,4'-didodecyl-2,2'-bithiopheneHCID 6712082085%

Reaktionsbedingungen

Temperatur0 °C

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUSRE044304E1
Quelldatensatzuspto-grants-2013_06
ORD IDord-76cd16eac47841e4bc50a1a442274da4
Quellennotizuspto-grants-2013_06