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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Isopropyl iodide | HCID 6362 | — |
| Reactant | Hexamethylphosphoramide | HCID 12679 | — |
| Reactant | 5-bromo-1-oxoindene | HCID 11367791 | — |
| Reactant | HCID 178418244 | HCID 178418244 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5-Bromo-2,3-dihydro-2-(1-methylethyl)-1H-inden-1-one | HCID 23158340 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07902369B2 |
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| Source dataset | uspto-grants-2011_03 |
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| ORD ID | ord-29960a3fe73d4452940101a44302149c |
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| Source note | uspto-grants-2011_03 |
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