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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 427697Generated: October 29, 2026

4-Chlorobenzoyl chloride → N1-(4-tert-Butylbenzoyl)-N2-(4-chlorobenzoyl)-1,2-benzenediamine

https://huagongshe.com/reaction/427697

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chlorobenzoyl chlorideHCID 8501—
ReactantPotassium CarbonateHCID 11430—
ReactantSodium HydroxideHCID 14798—
ReactantN-(2-aminophenyl)-4-tert-butylbenzamideHCID 1133079—
SolventDiethyl EtherHCID 3283—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
ProductN1-(4-tert-Butylbenzoyl)-N2-(4-chlorobenzoyl)-1,2-benzenediamineHCID 1052542966.4%

Reaction Steps

To a solution of N1-(4-tert-butylbenzoyl)-1,2-benzenediamine (100 mg, 0.37 mmol) in 3 mL methylene chloride was added 4-chlorobenzoyl chloride (95 μL, 0.74 mmol) and excess potassium carbonate. The mixture was stirred 30 min then a 1:1 solution of tetrahydrofuran and 5 N NaOH was added. The resultant mixture was stirred an additional 20 min and diluted with ether. The mixture was washed twice with water, dried over magnesium sulfate, filtered and concentrated in vacuo. The residue was sonicated with hexane causing a precipitate to form which was collected by filtration and dried under vacuum to yield 100 mg (66%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06313122B1
Source datasetuspto-grants-2001_11
ORD IDord-ac8d227cb56f4dcfb424c9984fb1e632
Source noteuspto-grants-2001_11