HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 552998Generated: October 25, 2026
Potassium Iodide → HCID 10610741, compound
https://huagongshe.com/reaction/552998
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Chloroacetone | HCID 6571 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 18-Crown-6 | HCID 28557 | — |
| Reactant | Methyl 2-(2-nitrophenyl)acetate | HCID 520464 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 10610741 | HCID 10610741 | 51% |
Reaction Steps
A three-neck round bottom flask with magnetic stirrer was charged with crude (2-nitro-phenyl)-acetic acid methyl ester (7.23 g, 37.0 mmol), potassium carbonate (46.1 g, 33.3 mmol), 18-crown-6 (0.650 g), and potassium iodide (0.650 g) under an argon atmosphere. To the flask was added acetonitrile (80 mL) and the mixture heated at 70° C. for one hour. To the reaction was added chloroacetone (3.50 mL, 44.0 mmol) and the reaction stirred at 70° C. under argon for 18-20 hours. The reaction was cooled to room temperature and filtered through a pad of celite. The resulting filtrate was concentrated in vacuo to afford 9.64 g of crude material. Purification via flash chromatography (0-40% ethyl acetate/hexanes eluent) yielded 4.74 g of 2-(2-nitro-phenyl)4-oxo-pentanoic acid methyl ester (51%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07951950B2 |
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| Source dataset | uspto-grants-2011_05 |
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| ORD ID | ord-272c67885f4341759f6c4c0c5ff34356 |
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| Source note | uspto-grants-2011_05 |
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