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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 631276Generated: October 26, 2026

Potassium Carbonate → Methyl 5-(2-methoxyethoxy)-2-nitrobenzoate

https://huagongshe.com/reaction/631276

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2-Bromoethyl methyl etherHCID 80972—
ReactantMethyl 5-hydroxy-2-nitrobenzoateHCID 12922678—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductMethyl 5-(2-methoxyethoxy)-2-nitrobenzoateHCID 6663915177%

Reaction Conditions

Temperature60 °C

Reaction Steps

To methyl 5-hydroxy-2-nitrobenzoate (1.08 g, 5.5 mmol) in DMF (50 mL) was added potassium carbonate (1.52 g, 11 mmol) followed by 1-bromo-2-methoxyethane (1.55 mL, 16.4 mmol) and the mixture heated at 60° C. overnight. After cooling to room temperature, the reaction was diluted with H2O, extracted with EtOAc, and the organic layer washed with H2O and brine, dried over MgSO4, filtered, concentrated in vacuo, and purified by column chromatography (12-100% EtOAc/hexanes) to give methyl 5-(2-methoxyethoxy)-2-nitrobenzoate (1.08 g, 4.2 mmol, 77%). 1H NMR (300 MHz, DMSO-d6) δ 8.13 (d, 1H), 7.31 (s, 1H), 7.29 (d, 1H), 4.29 (dd, 2H), 3.86 (s, 3H), 3.68 (dd, 2H), 3.31 (s, 3H); LC-MS (ESI) m/z 256 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09320739B2
Source datasetuspto-grants-2016_04
ORD IDord-4b9350ccd437411bad96225df5d6e392
Source noteuspto-grants-2016_04