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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2078762Generated: October 26, 2026

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

https://huagongshe.com/reaction/2078762

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantN-bromobutanimideHCID 67184—
Reactant4,4'-Didodecyl-2,2'-bithiopheneHCID 21917265—
SolventAcetic acid chloroformHCID 21584526—
Product5-Bromo-4,4'-didodecyl-2,2'-bithiopheneHCID 6712082085%

Reaction Conditions

Temperature0 °C

Reaction Steps

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07928249B2
Source datasetuspto-grants-2011_04
ORD IDord-2a92a1e3edf1455490830238d1690034
Source noteuspto-grants-2011_04