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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1801574Generated: October 26, 2026

1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → (R)-3-bromo-4-chloro-N-(1-(3-chlorophenyl)ethyl)benzamide

https://huagongshe.com/reaction/1801574

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant(R)-1-(3-chlorophenyl)ethanamineHCID 2507697—
Reactant3-Bromo-4-chlorobenzoic acidHCID 2735544—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product(R)-3-bromo-4-chloro-N-(1-(3-chlorophenyl)ethyl)benzamideHCID 5980317499.9%

Reaction Steps

To a solution of 3-bromo-4-chlorobenzoic acid 31 (4.209 g, 17.9 mmol) in DMF (40 mL) at room temperature was added HOBT (3.31 g, 21.6 mmol) and EDCI (4.13 g, 21.5 mmol). The solution was stirred for 15 min and (R)-1-(3-chlorophenyl)ethanamine (2.92 g, 18.8 mmol) was added. The reaction mixture was stirred at room temperature for 14 h and diluted with EtOAc. The aqueous phase was extracted with EtOAc (1×), and the combined organic extracts were washed with water (2×), brine, dried over MgSO4, filtered, and concentrated in vacuo. Purification by flash column chromatography on silica gel (eluted with 20% to 40% EtOAc in hexanes) gave (R)-3-bromo-4-chloro-N-(1-(3-chlorophenyl)ethyl)benzamide 32 (6.659 g, 99.9% yield) as a white solid. Mass spectrum: calculated for C15H12BrCl2NO 371.0. found 372.0 (M++1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08349831B2
Source datasetuspto-grants-2013_01
ORD IDord-38ef82ce54214086bb39af890e917706
Source noteuspto-grants-2013_01