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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1879433Generated: October 30, 2026

1,2-Dibromoethane → 1-(4-Bromo-3-fluorophenyl)cyclopropane-1-carbonitrile

https://huagongshe.com/reaction/1879433

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DibromoethaneHCID 7839—
ReactantSodium HydroxideHCID 14798—
Reactant2-(4-Bromo-3-fluorophenyl)acetonitrileHCID 11600953—
CatalystTetrabutylammonium BromideHCID 74236—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
Product1-(4-Bromo-3-fluorophenyl)cyclopropane-1-carbonitrileHCID 11715667—

Reaction Steps

A solution of 4-bromo-3-fluorophenylacetonitrile (5 g, 23 mmoles) in toluene (20 ml) is added with 35 mmoles of 1,2-dibromoethane, a 50% NaOH aqueous solution (20 ml) and tetrabutylammonium bromide (1.6 g, 5 mmoles). The mixture is kept under stirring at room temperature for 5-12 hours, then diluted with water and extracted with ethyl acetate. The organic phase is washed with 1N HCl, then with brine, finally dried and concentrated under vacuum to give a brown solid, which is subjected to chromatography on a silica gel column (200 g), eluting with hexane-ethyl ether 1-1, to afford the product in the solid form.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08314268B2
Source datasetuspto-grants-2012_11
ORD IDord-9da71984f5df453bb3f30e8a5ecaa0c3
Source noteuspto-grants-2012_11