Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1710335Generated: November 2, 2026

Tetrapropylammonium → 4-(3-(4-tert-Butylphenyl)-2-oxoimidazolidin-1-yl)benzaldehyde

https://huagongshe.com/reaction/1710335

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrapropylammoniumHCID 9559—
ReactantMethyl morpholine oxideHCID 82029—
Reactant1-(4-tert-Butylphenyl)-3-(4-(hydroxymethyl)phenyl)imidazolidin-2-oneHCID 59456885—
SolventAcetonitrileHCID 6342—
Product4-(3-(4-tert-Butylphenyl)-2-oxoimidazolidin-1-yl)benzaldehydeHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07790707B2
Source datasetuspto-grants-2010_09
ORD IDord-7e0ec03df734456c9f3d96305423e8bd
Source noteuspto-grants-2010_09