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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 217292Generated: October 27, 2026

Sodium Hydroxide → 2-(Carboxymethyl)-4-nitrobenzoic acid

https://huagongshe.com/reaction/217292

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactant2-(1,3-Dimethoxy-1,3-dioxopropan-2-yl)-4-nitrobenzoic acidHCID 10590078—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
Product2-(Carboxymethyl)-4-nitrobenzoic acidHCID 717202523.3%

Reaction Steps

A solution of sodium hydroxide (5.0 g, 125 mmol) in water (60 mL) was added to a solution of dimethyl 2-(2-carboxy-5-nitrophenyl)malonate (7.0 g, 21.5 mmol) in methanol (60 mL) at room temperature. After the reaction solution was stirred at room temperature for 3 hours, methanol was distilled off. The resulting residue was acidified using 1N hydrochloric acid (11 mL). The suspension was extracted with ethyl acetate. The organic layer was washed with brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure to give a crude product. After the crude product was stirred in ethyl acetate (20 mL) at 70 to 80° C. overnight, the temperature was allowed to return to room temperature. The precipitate was collected by filtration, and dried under reduced pressure to give the title compound (1.13 g, 23%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08193351B2
Source datasetuspto-grants-2012_06
ORD IDord-df486528467a40439168e9efa63e6064
Source noteuspto-grants-2012_06