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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1257980Generated: October 25, 2026

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

https://huagongshe.com/reaction/1257980

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 numberUSRE044304E1
Source datasetuspto-grants-2013_06
ORD IDord-76cd16eac47841e4bc50a1a442274da4
Source noteuspto-grants-2013_06