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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1702141Generated: October 31, 2026

Water → HCID 54071723, compound

https://huagongshe.com/reaction/1702141

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDimethyl SulfateHCID 6497—
ReactantMethyl acetoacetateHCID 7757—
ReactantSodium NitriteHCID 23668193—
SolventMethanolHCID 887—
ProductHCID 54071723HCID 54071723—

Reaction Steps

To 200 ml of water were added 38 g of sodium nitrite together with 53 g of methyl acetoacetate. Under ice-cooling and stirring, 200 ml of 4 N-sulfuric acid were added dropwise over a period of about 1 hour. During this period, the temperature of the reaction mixture was maintained at 5°-8° C. The mixture was further stirred within this temperature range for 2.5 hours. Then, it was extracted twice with 300 ml portions of ethyl acetate and the extracts are combined and washed twice with a standard aqueous solution of sodium chloride. Then, a solution of 96.9 g of sodium carbonate in 1 l of water was divided into three portions and the methyl 3-oxo-2-hydroxyiminobutyrate was extracted from the ethyl acetate layer previously obtained (3 times). To the water layer (1 l) were added 200 ml of methanol and, under ice-cooling and stirring, 150 g of dimethyl sulfate were added dropwise over a period of 10 minutes. After the dropwise addition was completed, the mixture was stirred at room temperature for 1.5 hours. It was then extracted twice with 300 ml of ethyl acetate, washed with water and dried. The ethyl acetate layer was distilled off and the residue is cooled with ice, whereupon it solidified. This solid was collected by filtration and rinsed with a small amount of water. By this procedure was obtained methyl 3-oxo-2-methoxyiminobutyrate as white crystals. 52.3 g; m.p. 64.4° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04380541
Source datasetuspto-grants-1983_04
ORD IDord-057f627115db4066b99b6cf0b709ef8c
Source noteuspto-grants-1983_04