Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 369690Generated: October 28, 2026

Water → 1-[4-(3,3-Dichloroprop-2-enyloxy)-2,6-dichlorophenoxy]-4-bromobutane

https://huagongshe.com/reaction/369690

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant1,4-DibromobutaneHCID 8056—
ReactantPotassium CarbonateHCID 11430—
Reactant4-(3,3-Dichloro-2-propenyloxy)-2,6-dichlorophenolHCID 11346738—
SolventDimethylformamideHCID 6228—
Product1-[4-(3,3-Dichloroprop-2-enyloxy)-2,6-dichlorophenoxy]-4-bromobutaneHCID 2225714574%

Reaction Steps

A reaction vessel was charged with 22.67 g of 1,4-dibromobutane, 11.06 g of potassium carbonate and 200 ml of N,N-dimethylformamide, to which a solution of 20.16 g of 2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenol dissolved in 80 ml of N,N-dimethylformamide was slowly added dropwise. After stirring at room temperature for 24 hours, the reaction mixture was poured into water and extracted twice with 300 ml of diethyl ether. The diethyl ether layers were combined, washed with water, dried over anhydrous magnesium sulfate and then concentrated to give a crude product. The crude product was subjected to silica gel chromatography, which afforded 21.77 g of 3,5-dichloro-4-(4-bromobutyloxy)-1-(3,3-dichloro-2-propenyloxy)benzene (yield, 74%), nD25.0 1.5666.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06140274
Source datasetuspto-grants-2000_10
ORD IDord-0284182e24304690b7c489b639fcab6f
Source noteuspto-grants-2000_10