Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 335913Generated: October 23, 2026

Ethyl Acetate → 5-Bromo-2-(2-fluoro-4-methoxyphenoxy)benzoic acid

https://huagongshe.com/en/reaction/335913

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantCesium carbonateHCID 10796—
Reactant2,5-Dibromobenzoic acidHCID 11891—
Reactant2-Fluoro-4-methoxyphenolHCID 2774557—
SolventTolueneHCID 1140—
Product5-Bromo-2-(2-fluoro-4-methoxyphenoxy)benzoic acidHCID 57475638—

Reaction Steps

A three-neck RBF equipped with a reflux condenser and overhead stirrer was charged with 2-fluoro-4-methoxyphenol (14.24 g, 100 mmol), 2,5-dibromobenzoic acid (25.5 g, 91 mmol), EtOAc (0.446 mL, 4.55 mmol), copper (I) triflate toluene complex (2:1) (0.484 g, 2.27 mmol) and toluene (300 mL). Cesium carbonate (59.4 g, 182 mmol) was carefully added portion-wise. The mixture was stirred for 10 minutes at RT then heated at 95° C. for 3 hours. The toluene was cooled to RT then extracted twice with 300 ml of water. The combined water extracts were acidified with 6 N HCl at which time a precipitate formed. The mixture was extracted with EtOAc (3×500 mL) and the combined organic fractions were dried over sodium sulfate and concentrated in vacuo. The resulting solid was triturated with minimal 1:1 Hexanes:EtOAc and filtered. The collected solid was dried in vacuo to afford 5-bromo-2-(2-fluoro-4-methoxyphenoxy)benzoic acid as a grey solid. The mother liquors were set aside for later recrystallizatio. MS m/z=341.0 [M+H].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08883782B2
Source datasetuspto-grants-2014_11
ORD IDord-9c6014187a184102861b820fe5ea691e
Source noteuspto-grants-2014_11