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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 846477Generated: October 30, 2026

1-Bromohexane → HCID 54131860, compound

https://huagongshe.com/reaction/846477

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-BromohexaneHCID 8101—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 21734064HCID 21734064—
CatalystCopperHCID 23978—
SolventDimethylformamideHCID 6228—
ProductHCID 54131860HCID 5413186080%

Reaction Steps

To 4 ml of a DMF solution containing 97 mg (0.2513 mmol) of 2,2'-dihydroxy-5,5'-bis (2-ethoxycarbonylethyl) biphenyl and 363.7 μl (2.513 mmol) of hexyl bromide, there were added 41.6 mg (0.3109 mmol) of anhydrous potassium carbonate and a small amount of copper powder and the resulting mixture was agitated overnight at room temperature. The reaction mixture was filtered by suction through Celite to remove the solid matter and the filtrate was washed with ethyl acetate. After the solvent in the filtrate was evaporated off under reduced pressure, the evaporated residue was dissolved in chloroform. This solution was washed with dilute hydrochloric acid, dilute aqueous sodium bicarbonate, water and aqueous sodium chloride solution in this sequence and was dried by adding anhydrous sodium sulfate. The residue obtained after the solvent had been evaporated off was purified by silica gel column chromatography (with 10 g of WAKO-gel C-200, eluent: hexane and toluene/ethyl acetate of 100/1) to obtain 94.4 mg (0.2008 mmol, 80%) of 2-hexyloxy-2'-hydroxy-5,5'-bis (2ethoxycarbonylethyl) biphenyl as an oily product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05136090
Source datasetuspto-grants-1992_08
ORD IDord-389bcdcbc3824324afc7e062f7f7f0a4
Source noteuspto-grants-1992_08