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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1242277Generated: October 30, 2026

Triethylamine → 2-(3-Methoxy-prop-1-ynyl)-phenoxy-acetic acid ethyl ester

https://huagongshe.com/reaction/1242277

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant3-MethoxypropyneHCID 69393—
ReactantAcetic acid, (2-iodophenoxy)-, ethyl esterHCID 11808921—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418476HCID 178418476—
SolventAcetonitrileHCID 6342—
Product2-(3-Methoxy-prop-1-ynyl)-phenoxy-acetic acid ethyl esterHCID 67072272—

Reaction Steps

A three neck reaction flask was successively charged with 12.65 g (41.3 mmol) of the above prepared (2-iodo-phenoxy)-acetic acid ethyl ester, 128 ml of acetonitrile, 5.793 g (2 eq.) of 3-methoxy-1-propyne, 17.28 ml (3 eq.) of NEt3, 1.45 g (0.05 eq.) of (PPh3)2PdCl2, and 0.394 g (0.05 eq.) of CuI. After stirring for 4 h the bulk of the solvent was removed i. V. and the residue distributed between HCl and AcOEt. Washing of the organic layer with cold water and brine, drying over magnesium sulfate, and evaporation of the solvents, followed by flash chromatography (SiO2, hexane/AcOEt=8/2), yielded 9.54 g of the title compound as light brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07115611B2
Source datasetuspto-grants-2006_10
ORD IDord-7078bc1fa8c344589753faa635a55d3e
Source noteuspto-grants-2006_10