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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Diethyl Oxalate | HCID 7268 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Reactant | 1-Iodo-2-methyl-3-nitrobenzene | HCID 11536258 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-(2-Iodo-6-nitro-phenyl)-2-oxo-propionic acid | HCID 59250086 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08329682B2 |
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| Source dataset | uspto-grants-2012_12 |
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| ORD ID | ord-ece1f7ac453743f6a2599f29c3c1918d |
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| Source note | uspto-grants-2012_12 |
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