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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 591717Generated: November 4, 2026

4-Methylmorpholine → 2-Amino-4,6-dichlorobenzamide

https://huagongshe.com/reaction/591717

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
ReactantAmmonium HydroxideHCID 14923—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant4,6-Dichloroanthranilic acidHCID 290498—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
SolventTetrahydrofuranHCID 8028—
Product2-Amino-4,6-dichlorobenzamideHCID 20491022—

Reaction Steps

To a solution of 2-amino-4,6-dichloro-benzoic acid (4.12 g, 20.0 mmol) in THF (120 mL) were added EDCl (4.22 g, 22.0 mmol), HOBt (2.70 g, 20.0 mmol) and N-methylmorpholine (2.22 g, 22.0 mmol). The reaction mixture was stirred at room temperature for 20 minutes, then 50% (v/v) aqueous NH4OH solution (2.8 mL, 40.0 mmol) was added. The mixture was stirred for 20 hours at room temperature. The solvent was evaporated, the residue was taken in ethyl acetate (200 mL), and water (200 mL) was added. The organic phase was separated; the aqueous phase was extracted with ethyl acetate (200 mL). The combined organic phase was washed with water (100 mL), then brine (100 mL), and dried over anhydrous sodium sulfate. The solvent was evaporated and dried under vacuum to give 2-amino-4,6-dichloro-benzamide as an off-white solid. Yield: 3.83 g (93%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09238640B2
Source datasetuspto-grants-2016_01
ORD IDord-0cfc8e414aec4cd38148cb4792e3b013
Source noteuspto-grants-2016_01