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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 560267Generated: October 25, 2026

Acetic Acid → ethyl 3-(3-fluorophenyl)-2-hydroxyimino-3-oxopropanoate

https://huagongshe.com/reaction/560267

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantEthyl 3-(3-fluorophenyl)-3-oxopropanoateHCID 2063904—
ReactantSodium NitriteHCID 23668193—
SolventWaterHCID 962—
Productethyl 3-(3-fluorophenyl)-2-hydroxyimino-3-oxopropanoateHCID 178472892—

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 3-(3-fluoro-phenyl)-3-oxo-propionic acid ethyl ester (4.85 mmol) in acetic acid (1.90 mmol) is cooled to 10° C. and a solution of sodium nitrite (5.63 mmol) in water (0.68 mL) is added dropwise. The mixture is allowed to reach RT, stirred for 2 h, poured into water (10 mL) and cooled to 0° C. The precipitate is filtered off and dried by azeotropic removal of water with toluene to give crude 3-(3-fluoro-phenyl)-2-hydroxyimino-3-oxo-propionic acid ethyl ester which is dissolved in a mixture of acetic anhydride (1.38 mL) and acetic acid (1.80 mL). Sodium acetate (0.30 mmol), HgCl2 (0.01 mmol) and zinc powder (14.6 mmol) are added successively. The mixture is stirred under reflux for 1 h, cooled to RT and filtered and the residue is washed with ether. The filtrate is washed three times with water and once with aq. K2CO3 solution (1.0 M). The organic layer is dried over MgSO4 and concentrated in vacuo to give the desired crude product which is purified by FC (heptane to heptane/EtOAc 3/7). LC-MS: tR=0.82 min; [M+H]+=268.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08063099B2
Source datasetuspto-grants-2011_11
ORD IDord-11f627c8d377462f991a403d3b9192b6
Source noteuspto-grants-2011_11