Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 43594Generated: October 27, 2026

3-Methoxy-4-nitrobenzoic acid → N-(3-Methoxy-4-nitrobenzoyl)serine methyl ester

https://huagongshe.com/reaction/43594

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Methoxy-4-nitrobenzoic acidHCID 78764—
ReactantDiisopropylethylamineHCID 81531—
ReactantL-Serine, methyl ester, hydrochloride (1:1)HCID 2723730—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
ProductN-(3-Methoxy-4-nitrobenzoyl)serine methyl esterHCID 6754893969%

Reaction Steps

Dichloromethane (80 mL) was added to serine methyl ester hydrochloride (2.64 g, 17 mmol), 3-methoxy-4-nitrobenzoic acid (3 g, 15.2 mmol), WSC hydrochloride (3.83 g, 20 mmol), DMAP (0.18 g, 1.5 mmol) and N,N-diisopropylethylamine (2.58 g, 20 mmol), and the mixture was stirred at room temperature for one day. The reaction solution was washed with water and brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (elution solvent: ethyl acetate/hexane=1/2, 1/1, 2/1, 1/0) to obtain 3.11 g of the title compound as a colorless solid (69%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08536197B2
Source datasetuspto-grants-2013_09
ORD IDord-44b331cbf319449888b2dd62743014fb
Source noteuspto-grants-2013_09