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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2280406Generated: October 31, 2026

Acetonitrile → 3-(4-(Benzyloxy)-2-fluorophenyl)-3-oxopropanenitrile

https://huagongshe.com/reaction/2280406

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantAmmonium ChlorideHCID 25517—
Reactant4-(Benzyloxy)-2-fluorobenzoyl chlorideHCID 54057946—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product3-(4-(Benzyloxy)-2-fluorophenyl)-3-oxopropanenitrileHCID 6795895079%

Reaction Steps

Acetonitrile (1.66 mL, 31.7 mmol) was dissolved in dry THF (40 mL) and the mixture was cooled to −78 C. Butyllithium (2.5 M, 9.5 mL, 23.8 mmol) was added dropwise, and the resulting reaction mixture was stirred for 15 minutes. A solution of 4-(benzyloxy)-2-fluorobenzoyl chloride (2.1 g, 7.93 mmol) in THF was then added dropwise to the reaction mixture, and the resulting reaction mixture was stirred at −78 C for 40 minutes. Saturated ammonium chloride solution was then added carefully to the reaction mixture, and the resulting mixture was allowed to warm to room temperature. Next, the mixture was partitioned between water and EtOAc, and the organic portion was washed further with brine, then dried over sodium sulfate, and concentrated onto silica gel and purified by chromatography (gradient: 9:1 EtOAc:hexanes to 1:1 EtOAc:hexanes to 100% ethyl acetate) to give the title compound in 79% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09139532B2
Source datasetuspto-grants-2015_09
ORD IDord-dcf2e05deece4d6d8a017d95835c3307
Source noteuspto-grants-2015_09