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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 643791Generated: October 25, 2026

Sodium hydride → 5-(4'-Methyl-biphenyl-4-yloxymethyl)-furan-2-carboxylic acid ethyl ester

https://huagongshe.com/reaction/643791

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantEthyl 5-(chloromethyl)-2-furancarboxylateHCID 263166—
Reactant4-(4-Methylphenyl)phenolHCID 1382789—
SolventDimethylformamideHCID 6228—
Product5-(4'-Methyl-biphenyl-4-yloxymethyl)-furan-2-carboxylic acid ethyl esterHCID 5969498784%

Reaction Conditions

Temperature-5 °C

Reaction Steps

4′-Methyl-biphenyl-4-ol (Intermediate 5; 2.0 g, 10.9 mmol) was added to a suspension of sodium hydride (60% dispersion; 384 mg, 9.6 mmol) in N,N-dimethylformamide (30 mL) and the mixture was stirred at −5° C. for 20 min. A solution of 5-(chloro-methyl)-furan-2-carboxylic acid ethyl ester (1.6 g, 8.5 mmol) in N,N-dimethylformamide (60 mL) was added and the reaction mixture was stirred overnight at room temperature. The solvents were evaporated under reduced pressure and the residue was partitioned between water and ethyl acetate. The aqueous layer was extracted twice with ethyl acetate, and the combined organic layers were washed with water and brine, dried (sodium sulfate) filtered, evaporated and chromatographed, eluting with 0-50% methylene chloride/hexanes to give 5-(4′-methyl-biphenyl-4-yloxymethyl)-furan-2-carboxylic acid ethyl ester (2.4 g, 84%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07700632B2
Source datasetuspto-grants-2010_04
ORD IDord-f7f0024d58a14cc0bd87ea9de714635f
Source noteuspto-grants-2010_04