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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 861684Generated: October 30, 2026

Nitrogen → 4-[3-(4-Fluorophenoxy)phenyl]but-3-yn-2-ol

https://huagongshe.com/reaction/861684

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitrogenHCID 947—
ReactantDiisopropylamineHCID 7912—
ReactantTriphenylphosphineHCID 11776—
Reactant3-Butyn-2-olHCID 16239—
Reactant3-(4-Fluorophenoxy)iodobenzeneHCID 2737345—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystBis(acetonitrile)dichloropalladiumHCID 6093782—
Solventtert-Butyl methyl etherHCID 15413—
Product4-[3-(4-Fluorophenoxy)phenyl]but-3-yn-2-olHCID 19704522—

Reaction Steps

A 30-gallon, glass-lined reactor was charged with 3-(4-fluoro-phenoxy)-iodobenzene (10.0 kg), copper(I) iodide (60.6 g), triphenyl-phosphine (95.0 g), bis(acetonitrile)palladium(II) chloride, and methyl t-butyl ether (27 kg). The mixture was cooled to 0°-10° C. and 55% aqueous 3-butyn-2-ol (4.20 kg) was added. Diisopropylamine (3.8 kg) was added to initiate the reaction and N2 was bubbled up from the bottom valve for a few minutes to agitate the reaction mixture. The reaction mixture was agitated at 15°-25° C. for 1.5 hours and then quenched by addition of 28% aqueous ammonia (12 kg) and brine (30 kg). The layers were separated and the organic phase was washed sequentially with brine (35 kg), 10% aqueous HCl (18 kg), 10% aqueous NaHCO3 (18 kg), and brine (35 kg). The organic phase was then stirred for 45 minutes with anhydrous MgSO4 (1.5 kg), PWA carbon (1.0 kg), and Ultra Norit C (1.0 kg) and filtered to give a solution of 4-[3-(4-fluorophenoxy)phenyl]-3-butyn-2-ol in methyl t-butyl ether which was used in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05714633
Source datasetuspto-grants-1998_02
ORD IDord-b476f5ec91444ec994fdf10d7c9edf05
Source noteuspto-grants-1998_02