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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 846493Generated: October 30, 2026

1-Bromooctane → HCID 54448652, compound

https://huagongshe.com/reaction/846493

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-BromooctaneHCID 8140—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 21734062HCID 21734062—
CatalystCopperHCID 23978—
SolventDimethylformamideHCID 6228—
ProductHCID 54448652HCID 5444865291.4%

Reaction Steps

To 5 ml of a DMF solution containing 200 mg (0.5181 mmol) of 2,2'-dihydroxy-5,5'-bis (3-methoxycarbonylpropyl) biphenyl and 0.895 ml (5.181 mmol) of octyl 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 for 5 hours 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 dissolve din 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 15 g of WAKO-gel C-200, eluent: toluene and toluene/ethyl acetate of 100/1) to obtain 236 mg (0.4738 mmol, 91%) of 2-octyloxy-2'-hydroxy-5,5'-bis (3-methoxycarbonylpropyl) biphenyl as an oily product. 1H-NMR (CDCl3) δ (ppm): 0.87 (3H, t, CH3), 1.0-2.2 (16H, m, 8CH2), 2.36 (4H, t, 2CH2), 2.65 (4H, t, 2CH2), 3.66 (6H, s, 2CH3), 4.01 (2H, t, CH2), 6.61 (1H, s, OH), 6.8-7.3 (6H, m, arom-H) MS (FAB): 497 (M-H)-

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05136090
Source datasetuspto-grants-1992_08
ORD IDord-48787e090db842099bd8f540019aecda
Source noteuspto-grants-1992_08