Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1859668Generated: October 27, 2026

Hydrochloric Acid → 3-(3,5-Dichloro-phenylamino)-N-phenyl-benzamide

https://huagongshe.com/reaction/1859668

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthylmorpholineHCID 7525—
Reactant1,3-Dichloro-5-iodobenzeneHCID 76424—
Reactant3-AminobenzanilideHCID 84347—
CatalystCupric acetateHCID 8895—
SolventWaterHCID 962—
SolventChloroformHCID 6212—
SolventDimethylformamideHCID 6228—
Product3-(3,5-Dichloro-phenylamino)-N-phenyl-benzamideHCID 186262113%

Reaction Steps

A mixture of 3-amino-N-phenyl-benzamide (2.0 g, 9.4 mmol), 3,5-dichloroiodobenzene (2.65 g, 9.7 mmol), N-ethylmorpholine (1.1 g, 9.5 mmol), and copper(II) acetate (0.1 g, 0.6 mmol) in N,N-dimethylformamide (6 mL) was stirred under an inert atmosphere and heated to reflux. After 120 hours, the mixture was allowed to cool and was stirred into water (300 mL) and acidified with concentrated hydrochloric acid. The mixture was extracted with dichloromethane (300 mL) and the extract separated and washed successively with 2N hydrochloric acid, water, 0.5 M aqueous potassium carbonate, water, and saturated aqueous sodium chloride, then dried over MgSO4. The solution was filtered and stripped of solvent under reduced pressure to leave a solid residue which was subjected to chromatography on a column of silica gel in chloroform to afford the product (0.1 g); m.p. 164-165° C. after recrystallization from ethyl alcohol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06528528B2
Source datasetuspto-grants-2003_03
ORD IDord-4b1c5d0a6a5f4296829c2073d7c23dd3
Source noteuspto-grants-2003_03