Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 4-Chloroanisole | HCID 12167 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Catalyst | HCID 86668671 | HCID 86668671 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-Methoxybiphenyl | HCID 11943 | 90% |
Reaction Steps
To a rubber-capped Schlenk vessel was added K3PO4 (298.4 mg, 1.4 mmol). This equipment was dried with flame under vacuum and backfilled with nitrogen for three times. Then Pd(OAc) (2.7 mg, 0.012 mmol), dicyclohexyl(2,4,6-trimethoxyphenyl)phosphine tetrafluoroborate (11.0 mg, 0.024 mmol), phenyl bronic acid (99.8 mg, 98%, 0.80 mmol), and 0.5 mL of dioxane were added sequentially to the Schlenk vessel. After being stirred for about 5 min at room temperature, p-methoxyphenyl chloride (56.5 mg, 0.40 mmol), another 0.5 mL of dioxane, and 21.5 μL of water (21.5 mg, 1.2 mmol) were added sequentially in one portion. The resulting mixture was heated at 110° C. with a preheated oil bath. After 11 h, the reaction was complete as monitored by GC. The reaction mixture was then cooled and diluted by 10 mL of CH2Cl2 and filtered through a short column of silica gel (eluent: 2×10 mL of CH2Cl2). Evaporation and purification by chromatography (petroleum ether/ether=60/1) on silica gel afforded 4-Methoxybiphenyl (65.9 mg, 90%)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09006491B2 |
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| Source dataset | uspto-grants-2015_04 |
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| ORD ID | ord-79ff9245706149588ee5349fdaf64a44 |
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| Source note | uspto-grants-2015_04 |
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