Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2421342Generated: November 4, 2026

2-Bromophenol → 1-Bromo-2-(4-fluorophenethoxy)benzene

https://huagongshe.com/reaction/2421342

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-BromophenolHCID 7244—
ReactantTriphenylphosphineHCID 11776—
ReactantDiisopropyl diazene-1,2-dicarboxylateHCID 75555—
Reactant4-Fluorophenethyl AlcoholHCID 82068—
SolventTetrahydrofuranHCID 8028—
Product1-Bromo-2-(4-fluorophenethoxy)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 numberUS07956084B2
Source datasetuspto-grants-2011_06
ORD IDord-ceed2bd0ca0b4d46822262198fcbc17f
Source noteuspto-grants-2011_06