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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1165531Generated: October 29, 2026

3-Hydroxybenzoic Acid → 3-[4-(4-Fluorobenzoyl)phenoxy]benzoic acid

https://huagongshe.com/reaction/1165531

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Hydroxybenzoic AcidHCID 7420—
Reactant(4,4-Difluoro-1,5-cyclohexadien-1-yl)phenylmethanoneHCID 26985121—
Product3-[4-(4-Fluorobenzoyl)phenoxy]benzoic acidHCID 19862063—

Reaction Steps

As shown by reaction (1), 4,-4-difluorobenzophenone is reacted with 3-hydroxybenzoic acid to obtain 3-[4-(4-fluorobenzoyl)phenoxy]benzoic acid. The reaction is carried out in a suitable aprotic solvent, such as dimethylsulfoxide or N,N-dimethylformamide, under an inert atmosphere, at an elevated temperature of about 100° to 140° C. for about 8 to 64 hours. The 3-[4-(4-fluorobenzoyl)phenoxy]benzoic acid (A) is then reacted with 3-aminophenol, as shown by reaction (2) to obtain 3-[4-(3-aminophenoxybenzoyl)phenoxy]benzoic acid (B). This reaction is carried out in a suitable aprotic solvent, under an inert atmosphere, at an elevated temperature of about 100° to 140° C. for about 8 to 64 hours. At the end of the reaction period, the reaction mixture is cooled, then poured into water, which is then neutralized to precipitate the monomer (B). If desired, the crude monomer can be purified by recrystallization or by dissolving it in a suitable solvent and precipitating it from solution into a suitable non-solvent.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04910282
Source datasetuspto-grants-1990_03
ORD IDord-562a108a43f64c16beec00d86481ef95
Source noteuspto-grants-1990_03