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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1163548Generated: October 28, 2026

3-Nitrophenol → Diethyl 2-methyl-2-(3-nitrophenoxy)malonate

https://huagongshe.com/reaction/1163548

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-NitrophenolHCID 11137—
ReactantDiethyl bromomethylmalonateHCID 94944—
ReactantPotassium FluorideHCID 522689—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductDiethyl 2-methyl-2-(3-nitrophenoxy)malonateHCID 2206040280%

Reaction Steps

Diethyl 2-bromo-2-methylmalonate (1.0 g, 3.95 mmole) was added to a stirred suspension of potassium fluoride (0.57 g, 9.8 mmole) in dry DMF (5 mL). After stirring for 20 min at room temperature, 3-nitrophenol (0.55 g, 3.95 mmole) was added. The resulting mixture was stirred at 60° C. for 6 h, cooled to room temperature, diluted with water (30 mL) and extracted with ethyl acetate (3×200 mL). The organic layer was washed with aq. 1N NaOH (2×75 mL), dried over anhydrous Na2SO4, filtered and evaporated in vacuo to provide diethyl 2-methyl-2-(3-nitrophenoxy)malonate (0.89 g, 80%). 1H NMR (CDCl3): δ 7.92 (dd, 1H, J=2.3 and 8.2 Hz), 7.82 (t, 1H, J=2.3 Hz), 7.41 (t, 1H, J=8.2 Hz), 7.30 (dd, 1H, J=2.3 and 8.2 Hz), 4.28 (qt, 4H, J=7.0 Hz), 1.81 (s, 3H), 1.26 (t, 6H, J=7.0 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07820819B2
Source datasetuspto-grants-2010_10
ORD IDord-a286bcdca2464d57b1670e54448a42f3
Source noteuspto-grants-2010_10