Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 531415Generated: October 31, 2026

4-Methoxybenzaldehyde → 2-(4-Methoxyphenyl)-4,4,5,5-tetramethylimidazolidine-1,3-diol

https://huagongshe.com/reaction/531415

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethoxybenzaldehydeHCID 31244—
Reactant2,3-Butanediamine, N,N'-dihydroxy-2,3-dimethyl-HCID 84402—
SolventMethanolHCID 887—
Product2-(4-Methoxyphenyl)-4,4,5,5-tetramethylimidazolidine-1,3-diolHCID 5915537734%

Reaction Steps

A solution of 2,3-bis(hydroxylamino)-2,3-dimethylbutane (1.3 g, 8.8 mmol) and 4-methoxy-benzaldehyde (1.2 g, 8.8 mmol) in methanol (10 mL) was stirred at room temperature until reactants disappeared as TLC indicated. 1,3-Dihydroxy-2-(4-methoxyphenyl)-4,4,5,5-tetramethylimidazolidine was obtained by filtration, the filtrate was evaporated under reduced pressure to obtain the second crop of the title compound. The combined compound was then washed with petroleum ether and used for the next reaction (0.8 g, 34% yield). 1HNMR (400 MHz, DMSO): δ 7.63 (s, 1H), 7.32 (d, 1H, J=6.8), 6.87 (d, 1H, J=5.8), 4.42 (s, 1H), 3.72 (s, 3H), 1.06 (s, 3H), 1.02 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09353477B2
Source datasetuspto-grants-2016_05
ORD IDord-ee17644a366a4f00ab689546353cea28
Source noteuspto-grants-2016_05