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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 852392Generated: October 27, 2026

Triethylamine → 2-{4-[5-(3-Fluoro-phenyl)-pent-4-ynyloxyl]-2-methyl-phenoxy}-2-methyl-propionic acid

https://huagongshe.com/reaction/852392

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1-Fluoro-3-iodobenzeneHCID 70725—
Reactant2-Methyl-2-(2-methyl-4-pent-4-ynyloxy-phenoxy)-propionic acidHCID 86602542—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventAcetonitrileHCID 6342—
Product2-{4-[5-(3-Fluoro-phenyl)-pent-4-ynyloxyl]-2-methyl-phenoxy}-2-methyl-propionic acidHCID 1166782967.5%

Reaction Steps

A degassed (argon) solution of 0.098 g (0.44 mmol) 1-fluoro-3-iodobenzene in 4 ml acetonitrile was treated with 0.111 g (0.40 mmol) 2-methyl-2-(2-methyl-4-pent-4-ynyloxy-phenoxy)-propionic acid (example 26B]), 0.014 g (0.02 mmol) PdCl2(Ph3P)2, 0.004 g (0.02 mmol) of CuI and 0.17 ml (1.20 mmol) triethylamine. The reaction was stirred for 2.5 h and then extracted with chilled aqueous 10% KHSO4/ether (three times). The organic phases were washed with aqueous 10% NaCl, dried (Na2SO4) and evaporated. Purification was done by flash-chromatography on silica gel (1. n-heptane/EtOAc 4:1 and 2. CH2Cl2/MeOH 2%-10%). The pure fractions were evaporated, dissolved in ether and washed with aqueous 10% KHSO4/ether (three times). The organic phase was dried (Na2SO4) and evaporated to yield 0.10 g of the title compound as an orange viscous oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07253192B2
Source datasetuspto-grants-2007_08
ORD IDord-f8e2510ef1064bb69c498adac866f4db
Source noteuspto-grants-2007_08