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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 394857Generated: October 29, 2026

1,4-Dioxane → 1-[3-Chloro-4-(1,3-oxazol-2-yl)phenyl]-1-ethanone

https://huagongshe.com/reaction/394857

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-DioxaneHCID 31275—
ReactantLithium ChlorideHCID 433294—
Reactant2-(4-Bromo-2-chlorophenyl)-1,3-oxazoleHCID 22313782—
CatalystHCID 178418397HCID 178418397—
Product1-[3-Chloro-4-(1,3-oxazol-2-yl)phenyl]-1-ethanoneHCID 2231380077%

Reaction Steps

To a stirred solution of 2-(4-bromo-2-chlorophenyl)-1,3-oxazole (2.88 g, 11.14 mmol) in 1,4-dioxane (70 mL) were added tributhyl(1-ethoxyvinyl)tin (4.5 mL, 13.37 mmol), LiCl (1.18 g, 27.85 mmol) and tetrakis(triphenylphosphine)palladium(0) (1.28 g, 1.11 mmol) at room temperature under nitrogen. The mixture was heated at reflux temperature for 4 hours, and cooled down to room temperature, the solvent was removed under reduced pressure and the residue was dissolved in ethyl acetate (50 mL), washed with water (20 mL), dried over MgSO4 and concentrated in vacuo. The residue was dissolved in THF (30 mL) then 2N HCl (30 ml) was added at room temperature. After 2 hours, saturated NaHCO3 (100 mL) was added to the mixture. The mixture was extracted with ethyl acetate (300 mL) dried over MgSO4. Removal of the solvent, gave an oily residue, which was purified by flash chromatography eluting with ethyl acetate/hexane (1/4) to give title compound (1.891 g, 77% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06603008B1
Source datasetuspto-grants-2003_08
ORD IDord-6542ae1f2684469b8bcc6b6574bb5eac
Source noteuspto-grants-2003_08