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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1477470Generated: October 26, 2026

N-bromobutanimide → 1-(4-Amino-3-bromo-phenyl)-cyclopropanecarbonitrile

https://huagongshe.com/reaction/1477470

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant1-(4-Aminophenyl)cyclopropanecarbonitrileHCID 13826936—
SolventAcetonitrileHCID 6342—
SolventEthyl AcetateHCID 8857—
Product1-(4-Amino-3-bromo-phenyl)-cyclopropanecarbonitrileHCID 6883826180.1%

Reaction Steps

To a solution of 1-(4-amino-phenyl)-cyclopropanecarbonitrile (96 mg, 0.60 mmol) in MeCN (3 mL) at 0° C. was added NBS (108 mg, 0.60 mmol) and the reaction was allowed to stir overnight. The reaction was diluted with EtOAc (25 mL) and was then washed with saturated aqueous NaHCO3 (1×25 mL). The organic layer was dried (Na2SO4) and concentrated in vacuo to give 114 mg (80%) of 1-(4-amino-3-bromo-phenyl)-cyclopropanecarbonitrile. The crude product was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09403804B2
Source datasetuspto-grants-2016_08
ORD IDord-55e16492505e4c3c98431b9fc0e297aa
Source noteuspto-grants-2016_08