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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 846482Generated: October 30, 2026

Dimethylformamide → HCID 86746047, compound

https://huagongshe.com/reaction/846482

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantPhenethyl bromideHCID 7666—
ReactantPotassium CarbonateHCID 11430—
ReactantToluene ethylacetateHCID 21584019—
ReactantHCID 21734064HCID 21734064—
CatalystCopperHCID 23978—
SolventTolueneHCID 1140—
ProductHCID 86746047HCID 8674604786%

Reaction Steps

To 5 ml of a DMF solution containing 200 mg (0.5181 mmol) of 2,2'-dihydroxy-5,5'-bis (2-ethoxycarbonylethyl) biphenyl and 707.6 μl (5.181 mmol) of phenethyl bromide, there were added 85.8 mg (0.6217 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 20 g of WAKO-gel C-200, eluent: toluene and toluene/ethyl acetate of 100/1 and 50/1 to obtain 218.1 mg (0.4451 mmol, 86%) of 2-phenethyloxy-2'-hydroxy-5,5'-bis (2-ethoxy-carbonylethyl) biphenyl as an oily product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05136090
Source datasetuspto-grants-1992_08
ORD IDord-f6db0cf4d2ff4782a765ebe544b78d3e
Source noteuspto-grants-1992_08