HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1247704Generated: October 25, 2026
Iodine → Di-tert-butyl(1-methyl-2,2-diphenylcyclopropyl)phosphane
https://huagongshe.com/reaction/1247704
Participants
| Role | Name | HCID | Charge |
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| Reactant | Iodine | HCID 807 | — |
| Reactant | Lithium Bromide | HCID 82050 | — |
| Reactant | Di-tert-butylchlorophosphine | HCID 139566 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Reactant | 1-Chloro-1-methyl-2,2-diphenylcyclopropane | HCID 12869608 | — |
| Catalyst | Copper iodide | HCID 83717 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | Di-tert-butyl(1-methyl-2,2-diphenylcyclopropyl)phosphane | HCID 21909131 | 25.2% |
Reaction Steps
Under a nitrogen atmosphere, 1-chloro-1-methyl-2,2-diphenylcyclopropane (2.43 g, 10.0 mmol), magnesium (0.279 g, 11.5 mmol) and THF (10 ml) were placed in a reaction flask, followed by addition of a trace amount of iodine and stirring at 60° C. for 5 hours. After cooling, copper iodide (1.92 g, 10.0 mmol), lithium bromide (0.879 g, 10.1 mmol) and chlorodi-tert-butylphosphine (2.1 ml, 11.0 mmol) were added and the resulting mixture was stirred at 60° C. for 3 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% (w/w) aqueous ammonia and a brine, and dried over anhydrous magnesium sulfate. The solvent was removed under reduced pressure to give the title compound (0.89 g, 25%) as white crystal.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07129367B2 |
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| Source dataset | uspto-grants-2006_10 |
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| ORD ID | ord-9094c94026fc4014a56e9606ac7fa179 |
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| Source note | uspto-grants-2006_10 |
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