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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2422487Generated: November 2, 2026

Tetrahydrofuran → 7-[4-(1-Ethyl-1-hydroxy-propyl)-[1,2,3]triazol-1-ylmethyl]-4-(3-fluoro-phenyl)-chromen-2-one

https://huagongshe.com/reaction/2422487

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
Reactant3-Ethyl-1-pentyn-3-olHCID 22698—
Reactant7-(azidomethyl)-4-(3-fluorophenyl)-2H-chromen-2-oneHCID 59774874—
CatalystCopper iodideHCID 83717—
SolventEthyl AcetateHCID 8857—
Product7-[4-(1-Ethyl-1-hydroxy-propyl)-[1,2,3]triazol-1-ylmethyl]-4-(3-fluoro-phenyl)-chromen-2-oneHCID 25056365—

Reaction Steps

To a solution of 7-(azidomethyl)-4-(3-fluorophenyl)-2H-chromen-2-one (343 mg, 0.78 mmol) and 3-ethyl-1-pentyn-3-ol (80 mg, 0.71 mmol) in THF (7 mL) N,N-diisopropylethylamine (622 uL, 3.6 mmol) and copper iodide (204 mg, 1.07 mmol) were added. After overnight stirring, the reaction was diluted with ethyl acetate, filtered and washed with water and brine. The organic layer was then dried over MgSO4, filtered and concentrated. The crude residue obtained was purified by column chromatography (acetone/CH2Cl2 10:90) to afford the title compound. 1H NMR (400 MHz, acetone-d6): 7.89 (s, 1H), 7.7-7.6 (m, 1H), 7.53 (d, 1H), 7.45-7.32 (m, 4H), 7.27 (d, 1H), 6.42 (s, 1H), 5.79 (s, 2H), 3.78 (s, 1H), 2.0-1.74 (m, 4H), 0.78 (t, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07960409B2
Source datasetuspto-grants-2011_06
ORD IDord-0694b45e958743cdb7865996d34083f8
Source noteuspto-grants-2011_06