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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1618823Generated: November 2, 2026

Triethylamine → 4-Bromo-N-(2-(phenylamino)phenyl)benzamide

https://huagongshe.com/reaction/1618823

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantN-Phenyl-o-phenylenediamineHCID 68297—
Reactant4-Bromobenzoyl chlorideHCID 68515—
SolventDichloromethaneHCID 6344—
Product4-Bromo-N-(2-(phenylamino)phenyl)benzamideHCID 23094055—

Reaction Steps

To a solution of 4-bromo-benzoyl chloride (11 g, 50 mmol) in anhydrous dichloromethane (DCM) (100 ml), was added N-phenylbenzene-1,2-diamine (10.2 g, 55 mmol), then triethylamine (17 ml, 122 mmol) slowly. The whole mixture was then stirred at room temperature (r.t.) overnight. Subsequent filtration gave a white solid (Compound 8) (6.5 g). The filtrate was worked up with water (300 ml), and then extracted with DCM (300 ml) three times. The resulting organic phase was collected and dried over MgSO4, concentrated and recrystallized in DCM/hexanes to give another portion of white solid (Compound 8) (10.6 g). The total amount of product (Compound 8) was 17.1 g, in 93% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08771845B2
Source datasetuspto-grants-2014_07
ORD IDord-2228b29536c64355a1e8efabf50f4e43
Source noteuspto-grants-2014_07