Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2261967Generated: November 2, 2026

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

https://huagongshe.com/reaction/2261967

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 numberUS07846959B2
Source datasetuspto-grants-2010_12
ORD IDord-7fc179b902a543bd8de7ffce7c113cc7
Source noteuspto-grants-2010_12