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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1501273Generated: October 25, 2026

Phenol → 4-Bromo-2-chloro-1-(1-phenoxyethyl)benzene

https://huagongshe.com/reaction/1501273

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenolHCID 996—
ReactantTriphenylphosphineHCID 11776—
ReactantDiisopropyl diazene-1,2-dicarboxylateHCID 75555—
Reactant1-(4-Bromo-2-chlorophenyl)ethanolHCID 20258128—
SolventTetrahydrofuranHCID 8028—
Product4-Bromo-2-chloro-1-(1-phenoxyethyl)benzeneHCID 118562737—

Reaction Steps

A solution of 1-(4-bromo-2-chlorophenyl)ethanol (1.32 g, 5.6 mmol), phenol (525 mg, 5.6 mmol) and triphenylphosphine (2198 mg, 8.4 mmol) in tetrahydrofuran (30 mL) was stirred at room temperature for 0.5 hour. Diisopropyl azodicarboxylate (1695 mg, 8.4 mmol) was dropwise to the reaction mixture and was stirred at room temperature for 12 hours. The mixture was concentrated to give a residue. The residue was purified by column chromatography (silica gel, petroleum ethe/ethyl acetate=5:1) to give 4-bromo-2-chloro-1-(1-phenoxyethyl)benzene as a colorless oil (882 mg 54%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09206128B2
Source datasetuspto-grants-2015_12
ORD IDord-332dd4e13ffd47c88f39d1f35ed54d62
Source noteuspto-grants-2015_12