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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2186206Generated: October 31, 2026

4-Methoxybenzaldehyde → N-[(4-Methoxyphenyl)methylidene]hydroxylamine

https://huagongshe.com/reaction/2186206

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethoxybenzaldehydeHCID 31244—
ReactantHydroxyamine hydrochlorideHCID 443297—
ReactantSodium AcetateHCID 517045—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductN-[(4-Methoxyphenyl)methylidene]hydroxylamineHCID 94712115.4%

Reaction Steps

4-Methoxybenzaldehyde (10.0 g, 73.4 mmol) was dissolved in 200 mL of ethanol. A solution of hydroxyamine hydrochloride (6.38 g, 91.8 mmol) in 50 mL of H2O was added followed by a solution of sodium acetate (12.1 g, 146.8 mmol) in 50 mL of H2O. The mixture was stirred at room temperature under N2 for 12 h. The ethanol was removed in vacuo and the aqueous mixture was extracted with EtOAc. The EtOAc solution was washed with brine, dried over MgSO4, and concentrated to afford 12.8 g of light yellow oil. 1H NMR showed it was 80% pure (92% yield). This material was taken into the next step without further purification. (CDCl3): δ2.15 (s, 1H); 3.83 (s, 3H); 6.92 (d, 2H); 7.50 (d, 2H); 8.10 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06403620B1
Source datasetuspto-grants-2002_06
ORD IDord-0b6b4d844ddf406f92ccac9e8d043472
Source noteuspto-grants-2002_06