Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | tert-Butyl hydroperoxide | HCID 6410 | — |
| Reactant | Phenylsilane | HCID 12752 | — |
| Reactant | p-Toluenesulphonyl cyanide | HCID 87946 | — |
| Reactant | HCID 59627202 | HCID 59627202 | — |
| Catalyst | Cobalt | HCID 104730 | — |
| Product | HCID 59627247 | HCID 59627247 | 4.5% |
Reaction Steps
Cobalt catalyst 1 (1.32 mg, 0.002 mmol, 1 mol %) was dissolved in EtOH (8 mL; absolute) at rt under argon, (R)-1-((S)-1-(4-bromophenyl)ethyl)-4-(2-methylallyl)-4-phenyltetrahydropyrimidin-2(1H)-one (82.6 mg, 0.2 mmol), TsCN (54 mg, 0.3 mmol), tBuOOH (6 mg, 0.06 mmol), and PhSiH3 (21.6 mg, 0.2 mmol) were added. The resulting solution was stirred at rt for 3 h. The solvent was removed by evaporation, and the residue was purified by prep HPLC to afford 3-((R)-1-((S)-1-(4-bromophenyl)ethyl)-2-oxo-4-phenylhexahydropyrimidin-4-yl)-2,2-dimethylpropanenitrile (4 mg, 4.5%) as a white solid. 1H NMR (CD3OD): δ 1.24 (s, 3H), 1.36 (s, 3H), 1.47-1.48 (m, 3H), 2.04-2.07 (m, 2H), 2.07 (m, 1H), 2.22-2.26 (m, 2H), 2.98-3.02 (m, 1H), 5.65-5.67 (m, 1H), 6.95-6.97 (m, 1H), 7.25-7.30 (m, 3H), 7.33-7.37 (m, 4H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09079861B2 |
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| Source dataset | uspto-grants-2015_07 |
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| ORD ID | ord-b28e4256e2644f609f32cb5a12358d19 |
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| Source note | uspto-grants-2015_07 |
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