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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1297013Generated: October 30, 2026

2-Bromothiophene → 2-Phenylthiophene

https://huagongshe.com/reaction/1297013

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-BromothiopheneHCID 13851—
ReactantPotassium FluorideHCID 522689—
ReactantHCID 178419127HCID 178419127—
Catalystpalladium(II) acetateHCID 167845—
Catalyst2-(Di-tert-butylphosphino)biphenylHCID 2734215—
SolventTetrahydrofuranHCID 8028—
Product2-PhenylthiopheneHCID 6999999.2%

Reaction Steps

An oven dried Schlenk tube was evacuated and backfilled with argon and charged with palladium acetate (2.2 mg, 0.01 mmol, 1.0 mol %), 2-(di-tert-butylphosphino)biphenyl (6.0 mg, 0.020 mmol, 2.0 mol %), phenylboron dihydroxide (183 mg, 1.5 mmol), and potassium fluoride (174 mg, 3.0 mmol). The tube was evacuated and backfilled with argon, and THF (1 mL) and 2-bromothiophene (0.097 mL, 1.0 mmol) were added through a rubber septum. The reaction mixture was stirred at room temperature until the starting aryl bromide had been completely consumed as judged by GC analysis. The reaction mixture was then diluted with ethyl acetate (30 mL) and poured into a separatory funnel. The mixture was washed with 2.0M NaOH (20 mL). The organic layer was washed with brine (20 mL), dried over anhydrous magnesium sulfate, filtered, and concentrated. The crude material was purified by flash chromatography on silica gel to afford 159 mg (99%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07247731B2
Source datasetuspto-grants-2007_07
ORD IDord-24f77b02c24c40908f481afe3f3d434d
Source noteuspto-grants-2007_07