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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 490339Generated: October 29, 2026

Dimethylformamide → 4-(4'-Acetyl-biphenyl-4-yloxymethyl)-5-methyl-furan-2-carboxylic acid

https://huagongshe.com/reaction/490339

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantPotassium AcetateHCID 517044—
Reactant4-Acetylphenylboronic acidHCID 3702122—
Reactant4-(4-Iodo-phenoxymethyl)-5-methyl-furan-2-carboxylic acid methyl esterHCID 58824157—
CatalystBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
SolventDichloromethaneHCID 6344—
Product4-(4'-Acetyl-biphenyl-4-yloxymethyl)-5-methyl-furan-2-carboxylic acidHCID 1844455720.4%

Reaction Conditions

Temperature90 °C

Reaction Steps

A stirred mixture of 4-(4-iodo-phenoxymethyl)-5-methyl-furan-2-carboxylic acid methyl ester (20) (0.26 g), 4-acetylphenylboronic acid (0.15 g), N,N-dimethylformamide (30 mL), potassium acetate (0.26 g) and [1,1′-bis(diphenylphosphino) ferrocene]dichloropalladium(II), complex with dichloromethane (1:1) (40 mg) was heated at 90° C. over night. The reaction mixture was concentrated in vacuo, dissolved in ethyl acetate (30 mL) and washed successively with water (30 mL), brine (30 mL), dried and concentrated in vacuo. The residue was dissolved in a mixture of tetrahydrofuran/methanol (2:1 by volume) (30 mL) and 1.0 M aqueous lithium hydroxide solution (6.78 mL) and stirred for 16 hours. The reaction mixture was acidified to pH 2 using 0.1M hydrochloric acid and extracted with ethyl acetate (3×25 mL). The extract was dried, concentrated in vacuo and the residue purified by HPLC to give compound 21 as a white solid (50 mg). LC/MS System C: Rt=4.18 mins, m/z (ES−)=349 (M− for C21H18O5).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07528157B2
Source datasetuspto-grants-2009_05
ORD IDord-7ecac089958642edbb367999d0f94465
Source noteuspto-grants-2009_05