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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2367121Generated: October 31, 2026

Water → Methyl 2-[(4-amino-3-nitrophenyl)carbonyl]benzoate

https://huagongshe.com/reaction/2367121

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantMethyl iodideHCID 6328—
ReactantCesium carbonateHCID 10796—
Reactant2-(4-Amino-3-nitrobenzoyl)benzoic acidHCID 2797522—
SolventDimethylformamideHCID 6228—
ProductMethyl 2-[(4-amino-3-nitrophenyl)carbonyl]benzoateHCID 14994663—

Reaction Steps

A solution of 2-[(4-amino-3-nitrophenyl)carbonyl]benzoic acid (10 g, 35 mmol) in DMF (50 mL) was treated with cesium carbonate (23 g, 70 mmol) followed by iodomethane (2.2 mL, 35 mmol). The mixture was stirred at rt for 1 h, after which time 50 mL of water was added. A yellow precipitate formed. The solid was collected by filtration, rinsed with water, and dried in vacuo. Desired methyl 2-[(4-amino-3-nitrophenyl)carbonyl]benzoate was obtained as a yellow solid (8.36 g, 27.8 mmol, 80% yield). 1H NMR (400 MHz, d6-DMSO): 8.12 (br s, 2H), 8.10 (d, 1H), 7.78-7.75 (m, 2H), 7.70 (m, 1H), 7.48 (dd, 1H), 7.10 (d, 1H), 3.64 (s, 3H); MS (EI) for C15H12N2O5: 323 (MNa+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08697737B2
Source datasetuspto-grants-2014_04
ORD IDord-0ba018c9dfd1464eabb076f08dccc258
Source noteuspto-grants-2014_04