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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 601649Generated: October 30, 2026

Isopropyl iodide → 5-Bromo-2,3-dihydro-2-(1-methylethyl)-1H-inden-1-one

https://huagongshe.com/reaction/601649

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsopropyl iodideHCID 6362—
ReactantHexamethylphosphoramideHCID 12679—
Reactant5-bromo-1-oxoindeneHCID 11367791—
ReactantHCID 178418244HCID 178418244—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product5-Bromo-2,3-dihydro-2-(1-methylethyl)-1H-inden-1-oneHCID 23158340—

Reaction Conditions

Temperature-78 °C

Reaction Steps

Under nitrogen atmosphere, 100 mg of 5-bromo-1-oxoindene was dissolved in 2 ml of tetrahydrofuran, and cooled down to −78° C. 0.4 ml of hexamethylphosphoramide, 0.3 ml of 1.57 M n-butyllitium hexane solution, and 1.0 ml of isopropyl iodide were added, and the mixture was stirred at −78° C. for 2 hours. Water was added to the reaction solution, and the mixture was extracted with ethyl acetate. Ethyl acetate layer was washed with saturated saline solution, and dried with anhydrous sodium sulfate. The solvents were distilled outunder reduced pressure, and the residues were separated and purified by preparative thin-layer chromatography (ethyl acetate/hexane=1/2) to obtain 26 mg of the above compound as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07902369B2
Source datasetuspto-grants-2011_03
ORD IDord-29960a3fe73d4452940101a44302149c
Source noteuspto-grants-2011_03