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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1523264Generated: November 2, 2026

Ethanol → HCID 59627247, compound

https://huagongshe.com/reaction/1523264

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
Reactanttert-Butyl hydroperoxideHCID 6410—
ReactantPhenylsilaneHCID 12752—
Reactantp-Toluenesulphonyl cyanideHCID 87946—
ReactantHCID 59627202HCID 59627202—
CatalystCobaltHCID 104730—
ProductHCID 59627247HCID 596272474.5%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09079861B2
Source datasetuspto-grants-2015_07
ORD IDord-b28e4256e2644f609f32cb5a12358d19
Source noteuspto-grants-2015_07