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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1362708Generated: October 30, 2026

Bromine → 2-Bromo-5-fluoro-1-indanone

https://huagongshe.com/reaction/1362708

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromineHCID 24408—
Reactant5-Fluoro-1-indanoneHCID 136537—
SolventAcetic AcidHCID 176—
Product2-Bromo-5-fluoro-1-indanoneHCID 11031641—

Reaction Conditions

Temperature60 °C

Reaction Steps

Bromine (1.98 mL) was added to a solution of 5-fluoroindanone (5.53 g) in acetic acid (100 mL), and the reaction solution was stirred at 60° C. for 10 minutes. After allowing the reaction solution to be cooled to room temperature, the solvent was evaporated under reduced pressure. Ethyl acetate and a saturated aqueous solution of sodium bicarbonate were added to the residue and the organic layer was partitioned. The resulting organic layer was dried over magnesium sulfate, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel chromatography (elution solvent: heptane-ethyl acetate system) to obtain 8.43 g of the title compound. The physical properties of the compound are as follows.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07880009B2
Source datasetuspto-grants-2011_02
ORD IDord-5d3cea6f42f8492db26b01385c083451
Source noteuspto-grants-2011_02