Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1176776Generated: October 30, 2026

Sodium Hydroxide → 5-[[4-(4-methylphenyl)phenoxy]methyl]furan-2-carboxylic Acid

https://huagongshe.com/reaction/1176776

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantTolylboronic acidHCID 79799—
ReactantMethyl 5-[(4-iodophenoxy)methyl]furan-2-carboxylateHCID 997605—
Catalystpalladium(II) acetateHCID 167845—
SolventWaterHCID 962—
Product5-[[4-(4-methylphenyl)phenoxy]methyl]furan-2-carboxylic AcidHCID 713885392.7%

Reaction Conditions

Temperature50 °C

Reaction Steps

A mixture of 5-(4-iodo-phenoxymethyl)-furan-2-carboxylic acid methyl ester (Intermediate 6; 100 mg, 0.28 mmol), 4-methyl-phenyl-boronic acid (42 mg, 0.31 mmol), sodium hydroxide (45 mg, 1.13 mmol), palladium(II) acetate (2 mg, 0.01 mmol) and water (10 mL) was heated at ˜50° C. overnight. The mixture was filtered and the residue was washed with water, ethyl acetate, methylene chloride, and methanol. The aqueous layer was acidified and extracted three times with ethyl acetate. The combined organic layers were washed with water and saturated brine, dried (magnesium sulfate), filtered, and evaporated to give 5-(4′-methyl-biphenyl-4-yloxymethyl)-furan-2-carboxylic acid (80 mg, 84%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07842825B2
Source datasetuspto-grants-2010_11
ORD IDord-bca941b5f22641f7af026f67826aa41e
Source noteuspto-grants-2010_11