Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Chloroanisole | HCID 12167 | — |
| Reactant | Cesium fluoride | HCID 25953 | — |
| Reactant | Phenylboronic Acid | HCID 66827 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 4-Methoxybiphenyl | HCID 11943 | 53% |
Reaction Steps
A 100 mL of reactor equipped with magnetic stir bar was charged with 140 mg (0.15 mmol) of {[(t-Bu)2P(OH)]2PdCl}2 (from Experiment 7), 1.43 g (10.0 mmol) of 4-chloroanisole, 1.83 g (15.0 mmol) of PhB(OH)2 and 4.56 g (30.0 mmol) of CsF in 30.0 mL of 1,4-dioxane. The resulting mixture was refluxed for 8 h until the starting material was completely consumed as judged by GC. The reaction was cooled to room temperature, transferred to a separatory funnel, and diluted with 300 mL of diethyl ether and 100 mL of H2O. The layers were separated, and organic layer was washed with H2O (2×100 mL), brine (100 mL), and dried over mgSO4, filtered, and the ether and dioxane removed from the filtrate by rotary evaporation. The resulting residue was chromatographed on silicon gel using 2% EtOAc/hexane as eluant. The eluate was concentrated by rotary evaporation followed by high vacuum to give 0.97 g (53% yield) of 4-phenylanisole.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06762330B2 |
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| Source dataset | uspto-grants-2004_07 |
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| ORD ID | ord-99b89c1da127425ba0fb0d2468611754 |
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| Source note | uspto-grants-2004_07 |
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