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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1671673Generated: October 31, 2026

Propanoic acid, 3-oxo-, methyl ester → HCID 178500960, compound

https://huagongshe.com/reaction/1671673

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropanoic acid, 3-oxo-, methyl esterHCID 182391—
ReactantSodium NitriteHCID 23668193—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
ProductHCID 178500960HCID 178500960—

Reaction Steps

A solution of the respective 3-oxo-propionic acid methyl ester derivative (4.8 mmol, 1.0 eq.) in glacial acetic acid (1.9 mL) was cooled to 10° C. and at this temperature was added a solution of NaNO2 (5.6 mmol, 1.16 eq.) in water (0.68 mL). After the addition was complete (15 min), the solution was allowed to warm to room temperature and stirred for 2 h. Then the solution was poured into water (10 mL) and after a few minutes crystals begun to appear. This suspension was cooled in an ice-bath and crystals were collected by filtration. The cake was washed several times with cold water and the water was removed by the azeotrope of toluene-water in vacuo to give 2-hydroxyimino-3-oxo-propionic acid methyl ester derivatives which were dissolved in a mixture of acetic anhydride (1.375 mL) and glacial acetic acid (1.8 mL). To this solution was added sodium acetate (0.296 mmol, 0.06 eq.) and HgCl2 (0.01 mmol, 0.002 eq.). The mixture was refluxed for 1 h, then cooled to room temperature and filtered. The solid was rinsed with ether, the organic filtrate was recovered, washed 3 times with water and one time with 1M aq. K2CO3. The organic layer was dried over MgSO4, filtered and concentrated. The crude products were purified by flash chromatography to afford the corresponding 2-acetylamino-3-oxo-propionic acid methyl ester derivatives.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07994336B2
Source datasetuspto-grants-2011_08
ORD IDord-06ebc9eff2cb4a039980f8d86fffb2b3
Source noteuspto-grants-2011_08