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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1487588Generated: October 26, 2026

Triethylamine → 4-Amino-3-chloro-N,N-dimethylbenzamide

https://huagongshe.com/reaction/1487588

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantDimethylamine, hydrochlorideHCID 10473—
Reactant4-Amino-3-chlorobenzoic acidHCID 17211—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
SolventIsopropanolHCID 3776—
SolventChloroformHCID 6212—
SolventDichloromethaneHCID 6344—
Product4-Amino-3-chloro-N,N-dimethylbenzamideHCID 2028748159.6%

Reaction Steps

To a solution of 4-amino-3-chlorobenzoic acid (1 equiv) in DCM (0.12 M) was added N-(3-dimethylaminopropyl)-N′-ethylcarbodiimide hydrochloride (1.2 equiv), 1-hydroxybenzotriazole (1.2 equiv), triethylamine (4 equiv) and dimethylamine hydrochloride (2 equiv) sequentially. The mixture was stirred at room temperature overnight. After the reaction was complete, as monitored by LCMS, the mixture was diluted with a mixture of isopropanol in chloroform (30%), washed with water and dried over anhydrous sodium sulfate. The organic phase was concentrated and the residue obtained was recrystallized in the mixture of hexane and ethyl acetate (10%) to afford the desired product (Yield: 59.6%) as a light brown solid. MS (ESI) m/z 199.1 [M+1]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09428509B2
Source datasetuspto-grants-2016_08
ORD IDord-d061683f71294405bc82d662ae7fa1c6
Source noteuspto-grants-2016_08