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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1176762Generated: October 25, 2026

4-Hydroxybiphenyl → Methyl 5-[(4-phenylphenoxy)methyl]furan-2-carboxylate

https://huagongshe.com/reaction/1176762

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-HydroxybiphenylHCID 7103—
ReactantSodium hydrideHCID 24758—
ReactantMethyl 5-(chloromethyl)-2-furoateHCID 75065—
SolventDimethylformamideHCID 6228—
ProductMethyl 5-[(4-phenylphenoxy)methyl]furan-2-carboxylateHCID 58691747,491.199%

Reaction Conditions

Temperature5 °C

Reaction Steps

N,N-Dimethylformamide (400 mL) was added to sodium hydride (60% dispersion; ˜16 g, 0.4 mol) which had been washed with hexanes. The mixture was cooled to ˜5° C., and then a solution of 4-phenylphenol (73.12 g, 0.43 mmol) in N,N-dimethylformamide (150 mL) was added. The mixture was allowed to stir at room temperature for 2.5 h, and then a solution of 5-chloromethylfuran-2-carboxylic acid methyl ester (25 g, 0.14 mmol) in N,N-dimethylformamide (100 mL) was added. The reaction mixture was heated at ˜105° C. for 2 h, and then it was allowed to cool, evaporated under reduced pressure, and water was added. The mixture was extracted three times with ethyl acetate, and the combined organic layers were washed with saturated brine, dried (magnesium sulfate), filtered, evaporated, and purified using a Biotage 75L purification system, eluting with 0-10% methylene chloride/toluene to give 5-(biphenyl-4-yloxymethyl)-furan-2-carboxylic acid methyl ester (20.5 g, 46%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07842825B2
Source datasetuspto-grants-2010_11
ORD IDord-fb9703d1b2a44b51813e87cec91f839a
Source noteuspto-grants-2010_11