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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2191519Generated: October 26, 2026

Ethanol → 3-(2-Iodo-6-nitro-phenyl)-2-oxo-propionic acid

https://huagongshe.com/reaction/2191519

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantDiethyl OxalateHCID 7268—
ReactantSodium ethoxideHCID 2723922—
Reactant1-Iodo-2-methyl-3-nitrobenzeneHCID 11536258—
SolventWaterHCID 962—
Product3-(2-Iodo-6-nitro-phenyl)-2-oxo-propionic acidHCID 59250086—

Reaction Conditions

Temperature100 °C

Reaction Steps

Sodium ethoxide solution (35 ml, 44 mmol) in an ice-water bath was added dropwise with a solution of 1-iodo-2-methyl-3-nitro-benzene 74b in ethanol (35 ml, 40 mmol) under an argon atmosphere. Upon completion of the addition, the reaction mixture was stirred until substantial brown precipitates were formed, and added with diethyl oxalate (6 ml, 44 mmol) in one portion. The reaction mixture was refluxed at 100° C. in an oil bath for 0.5 hour, added with water (70 ml) and refluxed for another 1 hour. The reaction mixture was concentrated under reduced pressure to evaporate ethanol, washed with ethyl acetate (50 ml) under base condition, adjusted to pH 3 with hydrochloric acid (1M), and extracted with ethyl acetate (30 ml×3). The combined organic extracts were washed with saturated brine (30 ml), dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure to obtain the title compound 3-(2-iodo-6-nitro-phenyl)-2-oxo-propionic acid 74c (2.94 g) as a brown oil to be used directly in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08329682B2
Source datasetuspto-grants-2012_12
ORD IDord-ece1f7ac453743f6a2599f29c3c1918d
Source noteuspto-grants-2012_12