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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 23376Generated: October 27, 2026

Methylparaben → 4-(4-Fluorophenoxy)benzoic acid

https://huagongshe.com/reaction/23376

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylparabenHCID 7456—
Reactant4-Fluorophenylboronic acidHCID 285645—
CatalystCupric acetateHCID 8895—
SolventDichloromethaneHCID 6344—
Product4-(4-Fluorophenoxy)benzoic acidHCID 500516391.9%

Reaction Steps

To a flask with 4-fluorophenyl boronic acid (2.1 g, 15 mmol), copper(II) acetate (1.4 g, 7.5 mmol), activated powdered molecular sieves (approximately 2 g), and methyl 4-hydroxybenzoate (1.2 g, 7.5 mmol) is added TEA (5.2 mL, 38 mmol) followed by CH2Cl2 (75 mL). The reaction is stirred for 16 hours at room temperature with air bubbling through it. The reaction mixture is diluted with CH2Cl2 and filtered through silica gel. The silica gel is washed with EtOAc-heptane. The solution is concentrated in vacuo and dissolved in dioxane (15 mL). To this solution is added aqueous LiOH (1N, 15 mL) and stirred for 18 hours at room temperature. To this reaction mixture is added aqueous HCl (1N) until acidic, having a pH less than 6. The resulting precipitate is collected by filtration and rinsed with water, and dried in vacuo to give 4-(4-fluorophenoxy)benzoic acid (1.6 g, 90%). MS for C13H9FO3 (ESI) (M−H)− m/z 231.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06852716B2
Source datasetuspto-grants-2005_02
ORD IDord-c99ce4ac2a264f8288ccd8735e8672e3
Source noteuspto-grants-2005_02