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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1648110Generated: October 31, 2026

1,5-Dibromopentane → HCID 54274067, compound

https://huagongshe.com/reaction/1648110

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,5-DibromopentaneHCID 8100—
ReactantPotassium CarbonateHCID 11430—
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
ReactantHCID 53904548HCID 53904548—
SolventMethyl Ethyl KetoneHCID 6569—
ProductHCID 54274067HCID 5427406783%

Reaction Conditions

Temperature90 °C

Reaction Steps

A mixture of 0.866 g (2.51 mmol) of 6-hydroxy-2,5-quinolinedipropanoic acid ethyl ester from the preceding example, 2.33 g (10.1 mmol) of 1,5-dibromopentane, 1.75 g (12.7 mmol) of anhydrous granular potassium carbonate and 25 mL of 2-butanone was stirred at 90° C. for 8.25 hr and at room temperature for another 37 hr. The mixture was filtered through anhydrous magnesium sulfate and the solids were washed with ethyl acetate. The filtrate and washes were combined and concentrated under reduced pressure. The residue was dissolved in 200 mL of ethanol, 1.21 g (6.36 mmol) of p-toluenesulfonic acid monohydrate was added and the resulting solution was stirred at room temperature for 22 hr. Most of the ethanol was removed under reduced pressure. The residue was treated with saturated aqueous sodium bicarbonate and worked-up with ethyl acetate in the usual manner. The crude product was partially purified by flash chromatography on 110 g of silica gel, eluting with hexane-ethyl acetate (3:1 and 2:1) giving 1.03 g of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05434186
Source datasetuspto-grants-1995_07
ORD IDord-beac2b12eb554889b4070cadee644df6
Source noteuspto-grants-1995_07