HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1474813Generated: October 28, 2026
Potassium Iodide → Ethyl 2-methyl-2-(3-nitrophenoxy)propanoate
https://huagongshe.com/reaction/1474813
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | 3-Nitrophenol | HCID 11137 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Propanoic acid, 2-bromo-2-methyl-, ethyl ester | HCID 11745 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Ethyl 2-methyl-2-(3-nitrophenoxy)propanoate | HCID 22060504 | — |
Reaction Steps
A mixture of 3-nitrophenol (0.50 g, 3.6 mmole), ethyl bromodimethylacetate (0.64 g, 3.3 mmole), K2CO3 (1.3 g, 9.4 mmole), potassium iodide (catalytic) in absolute ethanol (8 mL) was heated at 70° C. for 18 h. The reaction mixture was cooled, poured into a saturated solution of NaHCO3, and extracted with dichloromethane. The product, ethyl 2-methyl-2-(3-nitrophenoxyl)propanate, was obtained after purification by column chromatography over silica gel. 1H NMR (CDCl3): δ 7.85 (dt, 1H, J=1.2 and 8.1 Hz), 7.68 (t, 1H, J=2.4 Hz), 7.40 (t, 1H, J=8.4 Hz), 7.19-7.13 (m, 1H), 4.26 (q, 2H, J=7.2 Hz), 1.64 (s, 6H), 1.26 (t, 3H, J=7.21),
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09018204B1 |
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| Source dataset | uspto-grants-2015_04 |
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| ORD ID | ord-774695ae62da47c2a20bbc8064ad26bb |
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| Source note | uspto-grants-2015_04 |
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