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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 279152Generated: October 26, 2026

1-Indanone → 3-Bromo-1-indanone

https://huagongshe.com/reaction/279152

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-IndanoneHCID 6735—
ReactantN-bromobutanimideHCID 67184—
SolventCarbon TetrachlorideHCID 5943—
Product3-Bromo-1-indanoneHCID 11745912—

Reaction Steps

1-Indanone (1 g) and NBS (1.4 g) was mixed with dry CCl4 (20 ml). A catalytic amount of AlBN was added and the mixture was refluxed for 30 minutes and excited with light using 250 W lamp. The mixture was cooled in an ice bath and filtered. The filtrate was concentrated in an evaporator and used without further purification for the next step. Yield was 1.5 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06362211B1
Source datasetuspto-grants-2002_03
ORD IDord-c54a0fd89f4a4e89ae60c4b36eb93b67
Source noteuspto-grants-2002_03