Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Nitrogen | HCID 947 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Potassium vinyltrifluoroborate | HCID 23679353 | — |
| Reactant | HCID 66817913 | HCID 66817913 | — |
| Catalyst | HCID 178418807 | HCID 178418807 | — |
| Solvent | 1-Propanol | HCID 1031 | — |
| Product | HCID 66817208 | HCID 66817208 | — |
Reaction Steps
Potassium vinyltrifluoroborate (356 mg, 242 μmol), ethyldiisopropylamine (48 μL, 279 μmol) and [1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium dichloromethane adduct (15.1 mg, 18.6 μmol) were added to a solution of 3-(4-bromo-3-methyl-phenyl)-imidazolidine-2,4-dione (50 mg, 186 μmol) in n-PrOH (372 μL) at room temperature in an N2 atmosphere. The mixture was stirred at 100° C. for 1.5 hours, and the reaction solution was then cooled. The reaction solution was concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography (dichloromethane-methanol) to give 3-(3-methyl-4-vinyl-phenyl)-imidazolidine-2,4-dione as a yellow brown form (33 mg, 82%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09169254B2 |
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| Source dataset | uspto-grants-2015_10 |
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| ORD ID | ord-0ee1074a080a49e88de875a58a07ff28 |
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| Source note | uspto-grants-2015_10 |
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