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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1175089Generated: October 26, 2026

Water → 2-Bromo-3-[4-(2-ethylhexyl)-phenyl]-thiophene

https://huagongshe.com/reaction/1175089

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantN-bromobutanimideHCID 67184—
Reactant3-[4-(2-Ethylhexyl)-phenyl]-thiopheneHCID 59558257—
SolventDimethylformamideHCID 6228—
Product2-Bromo-3-[4-(2-ethylhexyl)-phenyl]-thiopheneHCID 59558252—

Reaction Steps

A 250-mL round bottom flask was charged with 3-[4-(2-ethylhexyl)-phenyl]-thiophene (7 g, 0.026 mol), N,N-dimethyl formamide (DMF) (65 mL). The reaction mixture was stirred at ambient temperature for 5 minutes, whereupon a 0.4 M solution of NBS (0.026 mol) in DMF was added and the stirring continued for 2 hours. After addition of water, the mixture was extracted with diethyl ether (3×150 mL). The combined organic layer was dried over anhydrous magnesium sulfate (MgSO4). After the product was filtered, the solvent was removed by rotary evaporation. The crude product was purified using column chromatography on silica gel with hexane as the eluent (Rf=0.35). The compound was dried under vacuum to yield 8.7 g (95%) of slightly yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07838624B2
Source datasetuspto-grants-2010_11
ORD IDord-e48e6f13ee674b4d92e35e3e140ab829
Source noteuspto-grants-2010_11