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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 23527Generated: October 30, 2026

3,4-Dichlorobenzoic acid → 3,4-Dichloro-N-methoxy-N-methylbenzamide

https://huagongshe.com/reaction/23527

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,4-Dichlorobenzoic acidHCID 5817—
Reactant4-MethylmorpholineHCID 7972—
ReactantMethanamine, N-methoxy-, hydrochloride (1:1)HCID 81138—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
Product3,4-Dichloro-N-methoxy-N-methylbenzamideHCID 1141364294.6%

Reaction Steps

To a suspension of 3,4-dichlorobenzoic acid (1.0 g, 5.24 mmol) in CH2Cl2 (25 mL) was added N,O-dimethylhydroxylamine hydrochloride (613 mg, 6.28 mmol) followed by N-methylmorpholine (865 μL, 7.85 mmol) and 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (1.2 g, 6.28 mmol) at which point the reaction mixture became homogeneous. After 2 h, the reaction mixture was diluted with EtOAc and washed with 1N HCl, H2O, saturated NaHCO3 solution and brine, sequentially. The organic layer was dried over Na2SO4, and the removal of solvent in vacuo gave the title compound (1.16 g) that required no further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06852727B2
Source datasetuspto-grants-2005_02
ORD IDord-387d71719b3a46319e14a0312e9bedf3
Source noteuspto-grants-2005_02