Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Morpholine | HCID 8083 | — |
| Reactant | 3-Bromostyrene | HCID 74870 | — |
| Reactant | Sodium t-butyloxide | HCID 86662868 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-(3-Vinyl-phenyl)-morpholine | HCID 22144974 | — |
Reaction Steps
Mixture of 3-bromo-styrene (11.2 g, 61.2 mmol), morpholine (123 mL), palladium acetate (343 mg, 2.5 mol %), di-t-butyl-biphenylphosphine (911 mg, 5 mol %), sodium t-butyloxide (6.47 g, 67.4 mmol) was stirred at 80° C. in a sealed tube for 30 minutes. After cooling down, the reaction mixture was diluted with dichloromethane (250 mL) and washed with water (100 mL). The aqueous layer was extracted with dichloromethane (2×125 mL) and the combined organic layer was dried over magnesium sulfate and concentrated under vacuum. The crude product was purified by Flash Chromatography of Biotage with 30% Ethyl Acetate/Hexanes. The title compound was obtained as pale yellow clear oil (10.7 g, 93% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07045551B2 |
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| Source dataset | uspto-grants-2006_05 |
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| ORD ID | ord-0f3ebebc36514c95ab35d3c792e48e40 |
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| Source note | uspto-grants-2006_05 |
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