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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2295918Generated: October 26, 2026

Toluene → beta-Oxo-alpha-phenyl-3-(trifluoromethyl)benzenebutanenitrile

https://huagongshe.com/reaction/2295918

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantPhenylacetonitrileHCID 8794—
ReactantMethyl (3-(trifluoromethyl)phenyl)acetateHCID 2734603—
ReactantSodium MethoxideHCID 10942334—
SolventMethanolHCID 887—
Productbeta-Oxo-alpha-phenyl-3-(trifluoromethyl)benzenebutanenitrileHCID 20474295—

Reaction Steps

To a flame-dried flask was added 8.1 g. of sodium methoxide, 125 ml. of toluene and 21 ml. of methanol. The mixture was brought to reflux at 85°-87°, and to it was added dropwise a mixture of 22.8 g. of methyl (3-trifluoromethylphenyl)acetate and 12.9 g. of phenylacetonitrile. The apparatus was then set up for distillation, and the mixture was heated to 110°, removing about 46 ml. of distillate. The mixture was then cooled to about 12°, and to it was added 50 ml. of ice-water. The aqueous layer was removed and washed with 20 ml. of cold toluene. The organics were combined and washed with cold water. The aqueous layers were combined, and the pH was adjusted to 3.5 with cold hydrochloric acid. The oily product was collected by extracting the aqueous portion with three 40 ml. portions of dichloromethane, drying the organic layer over sodium sulfate and evaporating it under vacuum to obtain 30.5 g. of oil, which was 89% pure product by vapor phase chromatography.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04426536
Source datasetuspto-grants-1984_01
ORD IDord-78ad4dfc3d2a4efe8e5ebbbae17fe5b0
Source noteuspto-grants-1984_01