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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 352072Generated: October 25, 2026

Toluene → 4-(acetoxymethyl)-2-[(E)-2-[4-(trifluoromethyl)phenyl]ethenyl]-1,3-oxazole

https://huagongshe.com/reaction/352072

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
Reactant1,3-DichloroacetoneHCID 10793—
Reactant4-(Trifluoromethyl)cinnamamideHCID 5709014—
ReactantSodium Acetate TrihydrateHCID 23665404—
SolventDimethyl SulfoxideHCID 679—
SolventMethanolHCID 887—
Product4-(acetoxymethyl)-2-[(E)-2-[4-(trifluoromethyl)phenyl]ethenyl]-1,3-oxazoleHCID 1299284665%

Reaction Conditions

Temperature72.5 °C

Reaction Steps

(E)-3-(4-(Trifluoromethyl)phenyl)-2-propenamide (10.0 g,46.5 mmol) and 1,3-dichloroacetone (11.0 g, 86.6 mmol) were added to toluene (50 ml), and the mixture was subjected to refluxing azeotropic dehydration using a Dean-Stark tube for 8.5 hours. The reaction mixture was concentrated under reduced pressure. To the residue were added dimethyl sulfoxide (50 ml) and sodium acetate trihydrate (15.8 g, 116.1 mmol). The mixture was stirred at 70-75° C. for 4 hours. Methanol (50 ml) was added. After allowing-to cool to room temperature and stirring; the mixture was stirred under ice-cooling for 1 hour. The precipitated crystals were collected by filtration, washed with cold-methanol (30 ml) and dried under reduced pressure to give 4-(acetoxymethyl)-2-[(E)-2-[4-(trifluoromethyl)phenyl]ethenyl]-1,3-oxazole (13.1 g, yield 65%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06743924B2
Source datasetuspto-grants-2004_06
ORD IDord-6c7a09e552c3430f98ac75e781c5f0fa
Source noteuspto-grants-2004_06