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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
Reactant3-NitrophenolHCID 11137—
ReactantPotassium CarbonateHCID 11430—
ReactantPropanoic acid, 2-bromo-2-methyl-, ethyl esterHCID 11745—
ReactantSodium BicarbonateHCID 516892—
SolventEthanolHCID 702—
ProductEthyl 2-methyl-2-(3-nitrophenoxy)propanoateHCID 22060504—

Reaction Conditions

Temperature70 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09018204B1
Source datasetuspto-grants-2015_04
ORD IDord-774695ae62da47c2a20bbc8064ad26bb
Source noteuspto-grants-2015_04