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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1491974Generated: October 26, 2026

Water → 2-(2-Phenoxyphenyl)-2-methoxyiminoacetamide

https://huagongshe.com/reaction/1491974

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantAmmonium HydroxideHCID 14923—
ReactantO-Methylhydroxylamine hydrochlorideHCID 521874—
ReactantMethyl 2-phenoxybenzoylformateHCID 13729870—
SolventMethanolHCID 887—
Product2-(2-Phenoxyphenyl)-2-methoxyiminoacetamideHCID 53967137—

Reaction Steps

To a solution of methyl-(2-phenoxyphenyl)-2-oxoacetate (0.70 g) in methanol (10 ml), 28% aqueous ammonium hydroxide (2.0 ml) was added, and the resultant mixture was stirred overnight, followed by removal of the solvent under reduced pressure. The residue was combined with diethyl ether (150 ml) and water (50 ml) under stirring and, upon dissolution, allowed to stand. The organic layer was separated, washed and dried over anhydrous sodium sulfate. Upon filtration, the filtrate was concentrated under reduced pressure to give residual yellow crystals, which were combined with methahol (10 ml) and O-methylhydroxylamine hydrochloride (1.49 g) while stirring and refluxed for 6 hours. Water (50 ml) was added to the reaction mixture, which was extracted with diethyl ether. The organic layer was washed with water and dried over anhydrous sodium sulfate, followed by filtration. The filtrate was concentrated under reduced pressure to give oily residue. The residue was purified by silica gel column chromatography with benzene to give 0.36 g of the objective compound. nD23.3 1.5978.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05371222
Source datasetuspto-grants-1994_12
ORD IDord-6a434bf132e74eb991b4337c9ec8ccfc
Source noteuspto-grants-1994_12