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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2357760Generated: November 1, 2026

Water → 3-Nitro-2-(phenylmethoxy)benzoic acid

https://huagongshe.com/reaction/2357760

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant3-Nitrosalicylic acidHCID 6807—
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
SolventDimethylformamideHCID 6228—
Product3-Nitro-2-(phenylmethoxy)benzoic acidHCID 22272669—

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of 2-hydroxy-3-nitrobenzoic acid (36.6 g) in N,N-dimethylformamide (500 mL) were added benzyl bromide (50.0 mL) and potassium carbonate (66.3 g), and the mixture was stirred overnight at 60° C. The reaction mixture was poured into water and the resulting mixture was extracted with a mixture of ethyl acetate and n-hexane (1:1). The organic layer was washed with water and saturated brine, dried over anhydrous sodium sulfate and concentrated. The residue was dissolved in a mixture of tetrahydrofuran (100 mL) and methanol (200 mL), and the resulting mixture was stirred for 30 minutes at 50° C. The reaction mixture was concentrated and the residue was acidified with 2N hydrochloric acid and extracted with ethyl acetate. The organic layer was washed with water and saturated brine, dried over anhydrous sodium sulfate and concentrated. The residue was recrystallized from isopropanol (50 mL)/n-hexane (200 mL) to give the title compound (31.99 g) having the following physical data.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07763610B2
Source datasetuspto-grants-2010_07
ORD IDord-c7dfdde8f48241e0b3e3453556ab0f4a
Source noteuspto-grants-2010_07