HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrapropylammonium → 4-(3-(4-tert-Butylphenyl)-2-oxoimidazolidin-1-yl)benzaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrapropylammonium | HCID 9559 | — |
| Reactant | Methyl morpholine oxide | HCID 82029 | — |
| Reactant | 1-(4-tert-Butylphenyl)-3-(4-(hydroxymethyl)phenyl)imidazolidin-2-one | HCID 59456885 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 4-(3-(4-tert-Butylphenyl)-2-oxoimidazolidin-1-yl)benzaldehyde | HCID 59456818 | — |
Reaction Steps
A mixture of 1-(4-tert-butylphenyl)-3-(4-(hydroxymethyl)phenyl)imidazolidin-2-one (100 mg, 0.31 mmol), 4-methylmorpholine N-oxide (72 mg, 0.62 mmol), and 4 A molecular sieves (100 mg) in 10 ml of acetonitrile was treated with tetrapropylammonium perruthnate and the resulting mixture was stirred at room temperature for 3 hours. The solids were filtered and the filtrated was concentrated. The residue was purified on ISCO system (2% methanol in dichloromethane) to give a pure product as a white crystalline (72 mg, 73%): 1H NMR (400 MHz, CDCl3) δ 9.93 (s, 1H), 7.81 (d, 2H), 7.79 (d, 2H), 7.50 (d, 2H), 7.40 (d, 2H), 4.03 (s, 4H), 1.33 (s, 9H). MS (ESI) m/z: Calculated: 322.17; Observed: 323.1 (M++1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07790707B2 |
| Source dataset | uspto-grants-2010_09 |
| ORD ID | ord-7e0ec03df734456c9f3d96305423e8bd |
| Source note | uspto-grants-2010_09 |