Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-(Dicyclohexylphosphino)biphenyl | HCID 2734216 | — |
| Reactant | 4,4,5,5-Tetramethyl[1,3,2]dioxaborolane | HCID 2734768 | — |
| Reactant | HCID 59350852 | HCID 59350852 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 67279752 | HCID 67279752 | — |
Reaction Steps
A mixture of the product from step (i) (6.6 g), 4,4,5,5-tetramethyl-[1,3,2]-dioxaborolane (1.94 ml), triethylamine (2.4 ml), palladium acetate (0.06 g) and 2-(dicyclohexylphosphino) biphenyl (0.3 g) in dioxane (20 ml) was heated at 85° C. for 2 h. The mixture was quenched with aqueous ammonium chloride solution, extracted with diethylether, the organics dried and evaporated under reduced pressure. The residue was purified by chromatography on silica eluting with 50% isohexane/DCM. Yield 0.7 g
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08158820B2 |
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| Source dataset | uspto-grants-2012_04 |
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| ORD ID | ord-1e82cc8060ed412482dc6da88f479bc0 |
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| Source note | uspto-grants-2012_04 |
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