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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1970083Generated: October 31, 2026

Thiophene → 2-(4-bromobutyl)-thiophene

https://huagongshe.com/reaction/1970083

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThiopheneHCID 8030—
Reactant1,4-DibromobutaneHCID 8056—
ReactantHexaneHCID 8058—
ReactantButyllithiumHCID 178418339—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product2-(4-bromobutyl)-thiopheneHCID 1142452950.7%

Reaction Steps

To a solution of thiophene (50 g, 594 mmol) in anhydrous THF (200 mL) is added slowly a 1.6M solution of n-butyllithium in hexane (408 mL, 653 mmol) under nitrogen atomospere at −30° C. The reaction mixture is stirred for a further 2 hours, during which period it is allowed to warm to room temperature. The solution is recooled to 0° C. and a solution of 1,4-dibromobutane (141 g, 653 mmol) in anhydrous THF (100 mL) is added. The stirring is continued overnight. The mixture is diluted with ethyl acetate (1000 mL) and shaken with water (800 mL). The organic layer is washed with brine twice and dried over anhydrous Na2SO4. After removal of the solvent, the residue is distilled in vacuo to afford 2-(4-bromobutyl)-thiophene 1 as colorless oil (66 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08426618B2
Source datasetuspto-grants-2013_04
ORD IDord-2bb2aeeae3c84f4d8fac734773a2f86c
Source noteuspto-grants-2013_04