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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 345865Generated: November 1, 2026

1,2-Dibromoethane → HCID 14798950, compound

https://huagongshe.com/reaction/345865

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DibromoethaneHCID 7839—
Reactant18-Crown-6HCID 28557—
ReactantBenzoylacetonitrileHCID 64799—
ReactantPotassium FluorideHCID 522689—
SolventDichloromethaneHCID 6344—
ProductHCID 14798950HCID 1479895020.9%

Reaction Steps

1 g (7 mmol) of α-cyanoacetophenone, 8 g (43 mmol) of 1,2-dibromoethane, 0.1 g (0.4 mmol) of 18-crown-6 and 4 g (69 mmol) of potassium fluoride are heated under reflux for 18 h as a heterogeneous system in 10 ml of dichloromethane. After cooling, the mixture is filtered, the organic phase is washed with H2O and the solvent is evaporated in vacuo after drying over Na2SO4. The residue is chromatographed on a silica gel using CH2Cl2. 0.25 g (20% of theory) of 1-benzoyl-1-cyanocyclopropane are obtained in this manner as a colorless oil,

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05059615
Source datasetuspto-grants-1991_10
ORD IDord-d1f5cbc4f007424b8ec05e31f4af6a49
Source noteuspto-grants-1991_10