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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 388190Generated: October 30, 2026

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

https://huagongshe.com/reaction/388190

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, 1 H), 7.32 (d, 1 H, J=6.8), 6.87 (d, 1 H, J=5.8), 4.42 (s, 1 H), 3.72 (s, 3 H), 1.06 (s, 3 H), 1.02 (s, 3 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08377670B2
Source datasetuspto-grants-2013_02
ORD IDord-cf814bd6504a4b24a85bc4bff699061f
Source noteuspto-grants-2013_02