Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Bromothiophene | HCID 13851 | — |
| Reactant | Potassium Fluoride | HCID 522689 | — |
| Reactant | HCID 178419127 | HCID 178419127 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Catalyst | 2-(Di-tert-butylphosphino)biphenyl | HCID 2734215 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Phenylthiophene | HCID 69999 | 99.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06946560B2 |
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| Source dataset | uspto-grants-2005_09 |
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| ORD ID | ord-34eb0c88d1d04acc935aed5366687059 |
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| Source note | uspto-grants-2005_09 |
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