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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 336246Generated: October 25, 2026

Bis(2-Methoxyethyl)amine → 4-[Bis(2-methoxyethyl)amino]-3-nitrobenzoic acid

https://huagongshe.com/reaction/336246

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBis(2-Methoxyethyl)amineHCID 2383—
Reactant4-Fluoro-3-nitrobenzoic acidHCID 67987—
SolventEthanolHCID 702—
Product4-[Bis(2-methoxyethyl)amino]-3-nitrobenzoic acidHCID 5960653894%

Reaction Steps

Bis(2-methoxyethyl)amine (Aldrich B4, 820-7; 1.6 g; 12 mmol; 3 eq.) was added to a solution of 4-fluoro-3-nitrobenzoic acid (740 mg; 4 mmol; 1 eq.) in EtOH (20 mL) and the resulting mixture was stirred at room temperature for 2 hours then at 70° C. for 20 hours. The solution was concentrated in vacuo and the residue was partitioned between NaOH 0.5M and Et2O. The aqueous layer was acidified to pH 2 with HCl 5M, extracted with ethyl acetate (3×) and the combined organic phase was dried over magnesium sulfate. After evaporation of the solvent, the residue was crystallised from ethyl acetate/n-pentane to afford the title compound (1.12 g, 94%) as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08889668B2
Source datasetuspto-grants-2014_11
ORD IDord-00eb722f19c94dcdbc595f22f6ef35f0
Source noteuspto-grants-2014_11