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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2206833Generated: October 31, 2026

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

https://huagongshe.com/reaction/2206833

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantN-Phenyl-o-phenylenediamineHCID 68297—
Reactant4-Bromobenzoyl chlorideHCID 68515—
SolventDichloromethaneHCID 6344—
Product4-Bromo-N-(2-(phenylamino)phenyl)benzamideHCID 2309405535.4%

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 (TEA) (17 ml, 122 mmol) slowly. The whole was stirred at room temperature (RT) overnight. Filtration gave a white solid 1 (6.5 g). The filtrate was worked up with water (300 ml), then extracted with DCM (300 ml) three times. The organic phase was collected and dried over MgSO4, concentrated and recrystallized in DCM/hexanes to give another portion of white solid 1 (10.6 g). Total amount of product 1 is 17.1 g, in 93% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09373797B2
Source datasetuspto-grants-2016_06
ORD IDord-4f38a1560ac44150be1a6d628ae8ab62
Source noteuspto-grants-2016_06