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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 422952Generated: October 29, 2026

4-Fluorophenol → 1-[(But-3-yn-1-yl)oxy]-4-fluorobenzene

https://huagongshe.com/reaction/422952

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-FluorophenolHCID 9732—
ReactantTriphenylphosphineHCID 11776—
Reactant3-Butyn-1-OLHCID 13566—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
SolventTetrahydrofuranHCID 8028—
Product1-[(But-3-yn-1-yl)oxy]-4-fluorobenzeneHCID 22279747—

Reaction Steps

To a solution of 4-fluorophenol (5.00 g, 44.6 mmol), 3-butyn-1-ol (3.38 ml, 44.6 mmol) and triphenylphosphine (17.5 g, 66.9 mmol) in tetrahydrofuran (100 ml) was added diethyl azodicarboxylate (11.7 g, 66.9 mmol) with stirring under ice-cooling, and then the resulting mixture was stirred at room temperature for 18 hours. After stirring, the reaction mixture was evaporated in vacuo, and to the residue were added hexane (200 ml) and ethyl acetate (20 ml). The precipitate separated out was filtered off, and the filtrate was evaporated in vacuo. The residue obtained was purified by flash chromatography on a silica gel column using hexane as the eluent to afford the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08101650B2
Source datasetuspto-grants-2012_01
ORD IDord-e7a5cfa946fb432b91a7cce2d9229e8f
Source noteuspto-grants-2012_01