HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1247701Erstellt: 24. Oktober 2026
Iodine → 2,2-Diphenyl-1-(diisopropylphosphino)-1-methylcyclopropane
https://huagongshe.com/de/reaction/1247701
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Iodine | HCID 807 | — |
| Edukt | Hexane | HCID 8058 | — |
| Edukt | (2-Bromo-1-phenylcyclopropyl)benzene | HCID 282328 | — |
| Edukt | Chlorodiisopropylphosphine | HCID 538967 | — |
| Edukt | Magnesium | HCID 5462224 | — |
| Katalysator | Copper iodide | HCID 83717 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 2,2-Diphenyl-1-(diisopropylphosphino)-1-methylcyclopropane | HCID 21909135 | 66% |
Reaktionsschritte
Under a nitrogen atmosphere, 1-bromo-2,2-diphenylcyclopropane (1.43 g, 5.0 mmol), magnesium (0.133 g, 5.5 mmol) and THF (10 ml) were placed in a reaction flask, followed by addition of a trace amount of iodine and stirring at 40° C. for 1.5 hours. After cooling, copper iodide (0.952 g, 5.0 mmol) and chlorodiisopropylphosphine (0.80 ml, 5.0 mmol) were added and the resulting mixture was stirred at 40° C. for 5 hours, followed by cooling to room temperature. The resulting mixture was diluted with hexane (20 ml) and crystal separated was collected by filtration. The crystal was dissolved in toluene, and the toluene solution was washed with a 28% aqueous ammonia and a brine, and dried over anhydrous magnesium sulfate. Then, the solvent was removed under reduced pressure to give the title compound (1.06 g, 66%) as white crystal.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07129367B2 |
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| Quelldatensatz | uspto-grants-2006_10 |
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| ORD ID | ord-c365289a83e448169295659bb3949063 |
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| Quellennotiz | uspto-grants-2006_10 |
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