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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 19537Generated: October 26, 2026

Azobisisobutyronitrile → 2-Bromo-3-phenyl-6-(3-phenylpropoxy)indene-1-one

https://huagongshe.com/reaction/19537

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzobisisobutyronitrileHCID 6547—
ReactantN-bromobutanimideHCID 67184—
Reactant3-Phenyl-6-(3-phenylpropoxy)indene-1-oneHCID 68694743—
CatalystTungstenHCID 23964—
SolventCarbon TetrachlorideHCID 5943—
Product2-Bromo-3-phenyl-6-(3-phenylpropoxy)indene-1-oneHCID 6869507660%

Reaction Steps

3-Phenyl-6-(3-phenyl-propoxy)-indene-1-one (200 mg, 0.586 mmol) obtained in Step 1 was dissolved in carbon tetrachloride, and N-bromosuccinimide (313 mg, 1.75 mmol) and 2,2′-azobisisobutyronitrile (9.7 mg) were added thereto. The mixture was refluxed for 1 hr under the irradiation of a 375 W tungsten lamp. Upon the completion of the reaction, the mixture washed with saturated saline and extracted with dichloromethane. The organic layer was separated, dried over anhydrous MgSO4 and concentrated under a reduced pressure. The resulting residue was purified by flash chromatography (ethyl acetate:hexane=1:5) to obtain 147 mg of the titled compound (yield: 60%) as a red solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07745439B2
Source datasetuspto-grants-2010_06
ORD IDord-93b0980d393d482f97ea807b4febef77
Source noteuspto-grants-2010_06