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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1777458Generated: October 29, 2026

Oxazole → 2-(4-Fluorophenyl)-1,3-oxazole

https://huagongshe.com/reaction/1777458

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxazoleHCID 9255—
Reactant4-FluoroiodobenzeneHCID 9605—
CatalystCopper iodideHCID 83717—
Catalystpalladium(II) acetateHCID 167845—
SolventDimethylformamideHCID 6228—
Product2-(4-Fluorophenyl)-1,3-oxazoleHCID 2103297725,539.1%

Reaction Steps

A solution of 1-fluoro-4-iodobenzene (1 g, 0.0144 mmol) in DMF (15 mL) was purged with argon, and oxazole (6.4 g/3.3 mL, 0.02898 mmol), copper iodide (5.5 g, 0.02898 mmol) and palladium (II) acetate (0.15 g, 0.000724 mmol) was added. The reaction mixture was purged with argon for 5 min and refluxed under argon for 12 h. The solution was cooled to room temperature and diluted with ice cold water (100 mL). The reaction mixture was extracted with ethyl acetate (200 mL) and filtered through Celite® reagent. The organic solvent was dried with sodium sulfate, filtered and the solvent was removed under reduced pressure to obtain crude product. The crude product was purified by Biotage IsoleraOne® column using a 25 g column (7% ethyl acetate in hexane) to give 2-(4-fluorophenyl)oxazole (0.6 g, 26%) as yellow liquid. 1H NMR (400 MHz, DMSO-d6): δ 8.19 (s, 1H), 8.03-7.99 (m, 2H), 7.34 (t, 3H); LC-MS m/z calculated for [M+H]+ 164.05. found 164.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09266873B2
Source datasetuspto-grants-2016_02
ORD IDord-7804a279b7ab4d6cb3f2ec8d15ca9dda
Source noteuspto-grants-2016_02