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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1674759Generated: November 1, 2026

Triphenylphosphine → 1-(2-(4-Bromo-3-fluorophenoxy)ethyl)-4-methylpiperazine

https://huagongshe.com/reaction/1674759

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantDiisopropyl diazene-1,2-dicarboxylateHCID 75555—
Reactant1-(2-Hydroxyethyl)-4-methylpiperazineHCID 231184—
Reactant4-Bromo-3-fluorophenolHCID 2779153—
SolventDichloromethaneHCID 6344—
Product1-(2-(4-Bromo-3-fluorophenoxy)ethyl)-4-methylpiperazineHCID 5900067533%

Reaction Steps

A flask was charged with 4-bromo-3-fluorophenol (5.00 g, 26 mmol) and triphenylphosphine (10.30 g, 39 mmol). Methylene chloride (120 mL) was added followed by 2-(4-methylpiperazin-1-yl)ethanol (4.61 g, 32 mmol) and the solution was stirred on an ice water bath to cool. After 5 minutes, diisopropyl azodicarboxylate (7.6 ml, 39.1 mmol) was added over 6 to 8 minutes. The reaction was left stirring on the cold bath to slowly warm to room temperature overnight. The reaction was concentrated and the residue purified by flash chromatography (25% to 100% EtOAc in hexanes) to provide the product as a colorless oil (2.62 g, 33%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08003641B2
Source datasetuspto-grants-2011_08
ORD IDord-dfded9296616424e84c12ef2d6b79f5e
Source noteuspto-grants-2011_08