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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1729276Generated: November 1, 2026

1,3-Dibromopropane → 1-(3-Bromopropoxy)-3-nitrobenzene

https://huagongshe.com/reaction/1729276

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-DibromopropaneHCID 8001—
Reactant3-NitrophenolHCID 11137—
ReactantPotassium CarbonateHCID 11430—
SolventMethyl Ethyl KetoneHCID 6569—
Product1-(3-Bromopropoxy)-3-nitrobenzeneHCID 717230194.7%

Reaction Steps

13.9 g of 3-nitrophenol, 101 g of 1,3-dibromopropane and 15.2 g of anhydrous potassium carbonate were reacted in 100 ml of methyl ethyl ketone for 2 hours by heating under reflux. After completion of the reaction, insoubles were removed from the reaction mixture by filtration, and the filtrate was then concentrated. Next, the resultant concentrate was dissolved in 300 ml of chloroform, and this chloroform solution was further washed with water. Afterward, the washed organic layer was dried over anhydrous magnesium sulfate and then treated with under reduced pressure to distill off the solvent, thereby obtaining 24.6 g of 3-(3-nitrophenoxy)propyl bromide (Compound d) in an oily state. This was used for a subsequent reaction without purifying.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05332739
Source datasetuspto-grants-1994_07
ORD IDord-c61f781d597e4c8686f29ee654da74eb
Source noteuspto-grants-1994_07