Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1004359Generated: October 29, 2026

Acetic Acid → HCID 178502837, compound

https://huagongshe.com/reaction/1004359

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantHydroxylamineHCID 787—
ReactantDimethylformamide dimethyl acetalHCID 78373—
ReactantHCID 86584673HCID 86584673—
SolventEthyl AcetateHCID 8857—
ProductHCID 178502837HCID 17850283775.6%

Reaction Conditions

Temperature60 °C

Reaction Steps

N,N-Dimethylformamide dimethylacetal (0.53 g, 4.5 mmol) was added to 2-(4-chlorophenoxymethyl)-α-methoxyiminophenylacetamide (0.48 g, 1.5 mmol), and the mixture was stirred under reduced pressure (ca. 40 mmHg) at 60° C. for 0.5 hours. After completion of the reaction, the mixture was concentrated under reduced pressure, and a mixture of aqueous 50% hydroxylamine solution (0.20 g, 2 mmol) and acetic acid (3 ml) was added to the residue under ice-cooling. The mixture was stirred at room temperature for 1 hour. After completion of the reaction, ethyl acetate (150 ml) was added, and the mixture was washed with saturated aqueous sodium bicarbonate solution (100 ml) twice. The ethyl acetate layer was dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue was recrystallized from ethyl acetate/n-hexane to give 2-(4-chlorophenoxymethyl)-N-hydroxyaminomethylene-α-methoxyiminophenylacetamide (0.41 g, 75.6%) as colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06048885
Source datasetuspto-grants-2000_04
ORD IDord-15c41e9f79b14d1dae3ee72ebfa21f5a
Source noteuspto-grants-2000_04