Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diglyme | HCID 8150 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 2-Bromoaniline | HCID 11992 | — |
| Reactant | Boronic Acid | HCID 61668 | — |
| Reactant | 4-Fluorophenylboronic acid | HCID 285645 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 4'-Fluoro(1,1'-biphenyl)-2-amine | HCID 2758975 | — |
Reaction Steps
To a stirred solution of 2-bromoaniline (1.72 g, 10.0 mmol) in diglyme (30 mL) tetrakis(triphenylphosphine)-palladium(0) (0.13 g, 0.3 mmol) and 2.0 M aqueous sodium carbonate solution (15 mL, 30.0 mmol) were added. In a separate flask, 4-fluorophenylboronic acid (2.23 g 16.0 mmol) was dissolved in ethanol (8 mL) and the mixture containing 2-bromoaniline was added to this boronic acid solution. The obtained brown reaction mixture was heated at 80° C. for 6 hours, then cooled, diluted with ethyl acetate and washed with saturated ammonium chloride solution. The organic layer was dried over sodium sulfate, filtered and concentrated. The residue was purified by flash column chromatography using Kieselgel 60 (0.015-0.040 mm) as adsorbent (Merck) and n-hexane:ethyl-acetate=2:1 as eluent to yield after recrystallization from ethanol 1.8 g (60%) of the title compound as white crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08034827B2 |
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| Source dataset | uspto-grants-2011_10 |
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| ORD ID | ord-bde24fca292d47739a7e6cad5611ac38 |
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| Source note | uspto-grants-2011_10 |
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