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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 6186Generated: October 25, 2026

1-Bromo-4-chlorobutane → 1,2-bis[N-(4-chlorobutyl)-N-propionylamino]benzene

https://huagongshe.com/reaction/6186

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Bromo-4-chlorobutaneHCID 81364—
ReactantN-[2-(propanoylamino)phenyl]propanamideHCID 694922—
CatalystTetrabutylammonium BromideHCID 74236—
SolventTolueneHCID 1140—
SolventSodium HydroxideHCID 14798—
Product1,2-bis[N-(4-chlorobutyl)-N-propionylamino]benzeneHCID 1907925412.6%

Reaction Steps

To a suspension of 3.27 g (15 mmol) of 1,2-di-propionylaminobenzene, 4.32 ml (37.5 mmol) of 4-bromo-1-chlorobutane, and 0.96 g (3.0 mmol) of tetrabutylammonium bromide in 25 ml of toluene, 5.6 ml of 50% aqueous sodium hydroxide was added at room temperature, and the mixture was stirred for 16 hours. The organic layer was separated, washed with saturated aqueous sodium chloride, and dried. The solvent was distilled off and the residue was purified by column chromatography (eluent: hexane/ethyl acetate =2 :1 to 1:1 to 1:2 to 1:4) to give 0.76 g of the desired product (12.6% yield, white crystals).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05246948
Source datasetuspto-grants-1993_09
ORD IDord-100d3d0cc94243f9be6bff4a345d975c
Source noteuspto-grants-1993_09