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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 557618Generated: October 26, 2026

1,2-Dibromoethane → 1-(Biphenyl-4-YL)-cyclopropanecarbonitrile

https://huagongshe.com/reaction/557618

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DibromoethaneHCID 7839—
ReactantEthyl AcetateHCID 8857—
ReactantPotassium HydroxideHCID 14797—
Reactant4-BiphenylacetonitrileHCID 35856—
CatalystTetrabutylammonium BromideHCID 74236—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
Product1-(Biphenyl-4-YL)-cyclopropanecarbonitrileHCID 6666052899.4%

Reaction Conditions

Temperature65 °C

Reaction Steps

4-phenyl-phenylacetonitrile (VWR scientific, 55.7 g, 289 mmol) was added to a solution of KOH (161.6 g, 2890 mmol) in water (170 mL) and toluene (550 mL) at room temperature. Tetrabutyl ammonium bromide (9.2 g, 29 mmol) followed by 1,2 dibromoethane (64.9 g, 347 mmol) were added and the solution was heated to 65° C. overnight. Reaction complete by TLC (10% EtOAc/hex). The organic layer was extracted 2 times with dilute hydrochloric acid, dried and evaporated to yield 63 g of 1-(biphenyl-4-yl)cyclopropanecarbonitrile.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08058300B2
Source datasetuspto-grants-2011_11
ORD IDord-0b724cd5e16b465b81f0a7b601e04b9c
Source noteuspto-grants-2011_11