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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1845797Generated: November 2, 2026

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

https://huagongshe.com/reaction/1845797

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 numberUS08951766B2
Source datasetuspto-grants-2015_02
ORD IDord-fd2cb89c47bd4815a409e6f444112bd5
Source noteuspto-grants-2015_02