Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Reactant | 3,3,5,5-Tetramethylcyclohex-1-en-1-yl triflate | HCID 11087380 | — |
| Reactant | 2-Dicyclohexylphosphino-2',6'-dimethoxybiphenyl | HCID 11269872 | — |
| Reactant | Methyl 2'-fluoro-5'-(methyloxy)-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1,1'-biphenyl-4-carboxylate | HCID 57706776 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 57706531 | HCID 57706531 | 58.7% |
Reaction Steps
A screw-cap vial was charged with 66.31A (0.556 g, 1.94 mmol), THF (10 mL), 66.56A (0.500 g, 1.29 mmol), potassium phosphate (0.824 g, 3.88 mmol), 2-dicyclohexylphosphino-2′,6′-dimethoxybiphenyl (commercially available from Aldrich) (0.165 g, 0.401 mmol), palladium(II) acetate (0.0291 g, 0.129 mmol), and water (0.117 mL, 6.47 mmol). The mixture was purged with argon and stirred for 48 hours at room temperature under an argon balloon. Additional 2-dicyclohexylphosphino-2′,6′-dimethoxybiphenyl (0.165 g, 0.401 mmol), palladium(II) acetate (0.0291 g, 0.129 mmol), and 69.31A (0.556 g, 1.94 mmol) were added, and stirring was continued for 16 hours at room temperature under argon. The mixture was filtered through silica gel (EtOAc) and concentrated. The crude product was purified by silica gel flash chromatography (0-5% EtOAc/hexane) to afford 69.31B (0.300 g, 58% yield) as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08030354B2 |
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| Source dataset | uspto-grants-2011_10 |
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| ORD ID | ord-88e265bc0dc8409d98c5a8dfe6001736 |
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| Source note | uspto-grants-2011_10 |
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