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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1245822Generated: October 31, 2026

2-Bromophenol → 1-Bromo-2-[2-(4-fluorophenyl)ethoxy]benzene

https://huagongshe.com/reaction/1245822

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-BromophenolHCID 7244—
ReactantTriphenylphosphineHCID 11776—
ReactantDiisopropyl diazene-1,2-dicarboxylateHCID 75555—
Reactant4-Fluorophenethyl AlcoholHCID 82068—
SolventTetrahydrofuranHCID 8028—
Product1-Bromo-2-[2-(4-fluorophenyl)ethoxy]benzeneHCID 2191434075.7%

Reaction Steps

2-Bromophenol (3.46 g) was mixed with tetrahydrofuran (60 ml) and triphenylphosphine (6.3 g) was added along with 4-fluorophenethyl alcohol (4.2 g). The mixture was cooled in an ice bath before dropwise addition of diisopropyl azodicarboxylate (4.85 g). The mixture was allowed to warm to room temperature over 18 h. The mixture was evaporated and diethyl ether (100 ml) was added. Stirring was continued for 3 h, the mixture was filtered and the filtrate was evaporated. The product was purified by column chromatography eluting with ethyl acetate/hexane mixtures to give a yellow oil (4.47 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07125896B2
Source datasetuspto-grants-2006_10
ORD IDord-907b4dfff61f407080ed1e9bfa8c5e05
Source noteuspto-grants-2006_10