Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1517673Generated: November 3, 2026

Azobisisobutyronitrile → 3-Bromo-5-methoxy-2,3-dihydro-1H-inden-1-one

https://huagongshe.com/reaction/1517673

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzobisisobutyronitrileHCID 6547—
ReactantN-bromobutanimideHCID 67184—
Reactant5-Methoxyindan-1-oneHCID 78787—
SolventCarbon TetrachlorideHCID 5943—
Product3-Bromo-5-methoxy-2,3-dihydro-1H-inden-1-oneHCID 23250651—

Reaction Conditions

Temperature85 °C

Reaction Steps

N-bromosuccinimide (12.1 g, 67.9 mmol) and 2,2′-azobisisobutyronitrile (0.1 g, 0.6 mmol) were added to a solution of 5-methoxy-1-indanone (10.0 g, 61.7 mmol) in carbon tetrachloride (104 mL). The reaction mixture was stirred for 3 hours at 85° C. and then allowed to cool to room temperature. The reaction mixture was filtered through Celite, which was then washed with CH2Cl2 (100 mL). The filtrate was washed with brine (50 mL), dried over MgSO4, and concentrated to afford the subtitle compound, which was used without further purification. MS calculated for C10H9BrO2+H: 241, observed: 241.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08232311B2
Source datasetuspto-grants-2012_07
ORD IDord-dfa8f72edb324b9f87e14bce8cf59c4b
Source noteuspto-grants-2012_07