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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1016569Generated: October 25, 2026

2-Chlorobenzyl chloride → N-acetyl-N-(2-chlorobenzyl)-2-phenoxyaniline

https://huagongshe.com/reaction/1016569

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chlorobenzyl chlorideHCID 11906—
ReactantSodium hydrideHCID 24758—
Reactant2-PhenoxyacetanilideHCID 897080—
SolventDimethylformamideHCID 6228—
ProductN-acetyl-N-(2-chlorobenzyl)-2-phenoxyanilineHCID 1840720694.3%

Reaction Steps

To a suspension of 400 mg of sodium hydride (60% in oil) in 30 ml of dimethylformamide was added 2.00 g of N-acetyl-2-phenoxyaniline at room temperature, followed by stirring at room temperature for 30 minutes. To the solution was added dropwise 1.64 g of 2-chlorobenzyl chloride at room temperature with stirring, followed by stirring for 30 minutes. After addition of ice-water, the reaction mixture was extracted with ether. The extract was washed with 0.5 N hydrochloric acid, a saturated aqueous sodium bicarbonate solution and a saturated aqueous sodium chloride solution, successively, and dried over anhydrous sodium sulfate. After removal of the drying agent by filtration, the solvent was concentrated under reduced pressure, and the residue was purified by silica gel column chromatography (eluent; ethyl acetate−hexane=1:4) to give 2.92 g of N-acetyl-N-(2-chlorobenzyl)-2-phenoxyaniline as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06476056B2
Source datasetuspto-grants-2002_11
ORD IDord-74ec7bab891f46928df49dd550016812
Source noteuspto-grants-2002_11