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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1085283Generated: October 30, 2026

1,3-Dibromopropane → HCID 20061406, compound

https://huagongshe.com/reaction/1085283

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-DibromopropaneHCID 8001—
ReactantPotassium CarbonateHCID 11430—
Reactant2,6-Dichloro-4-nitrophenolHCID 12066—
ReactantPotassium tert-butoxideHCID 23665647—
SolventMethyl Ethyl KetoneHCID 6569—
ProductHCID 20061406HCID 2006140694.8%

Reaction Steps

A mixture of 4.16 g of 2,6-dichloro-4-nitrophenol, 40.4 g of 1,3-dibromopropane, 2.76 g of potassium carbonate and 2.46 g of potassium t-butoxide was heated under reflux for 4 hours in 50 ml of methyl ethyl ketone. The reaction mixture was allowed to cool down and insoluble matters were filtered off. The filtrate was concentrated under reduced pressure. The residue was dissolved in chloroform. The thus-prepared chloroform solution was washed with water, and the chloroform was then distilled off. The residue was purified by chromatography on a silica gel column (eluent: chloroform/hexane=4/1, by volume) to obtain 6.24 g of 1-bromo-3-(2,6-dichloro-4-nitrophenyloxy)propane. This compound was employed in the next reaction without any further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05008267
Source datasetuspto-grants-1991_04
ORD IDord-0d2a0a8c0bf840bba81e04ba67592408
Source noteuspto-grants-1991_04