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HRID 1247702作成日:2026年10月27日

Iodine → Di-tert-butyl(1-methyl-2,2-diphenylcyclopropyl)phosphane

https://huagongshe.com/reaction/1247702

反応式

関与物質

役割名称HCID仕込み量
反応物IodineHCID 807—
反応物HexaneHCID 8058—
反応物Lithium BromideHCID 82050—
反応物Di-tert-butylchlorophosphineHCID 139566—
反応物(2-Bromo-1-phenylcyclopropyl)benzeneHCID 282328—
反応物MagnesiumHCID 5462224—
触媒Copper iodideHCID 83717—
溶媒TetrahydrofuranHCID 8028—
生成物Di-tert-butyl(1-methyl-2,2-diphenylcyclopropyl)phosphaneHCID 2190913147%

反応条件

温度40 °C

反応手順

Under a nitrogen atmosphere, 1-bromo-2,2-diphenyl-cyclopropane (1.44 g, 5.0 mmol), magnesium (0.134 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 one hour. After cooling, copper iodide (0.962 g, 5.0 mmol), lithium bromide (0.567 g, 6.5 mmol) and chlorodi-tert-butylphosphine (0.95 ml, 5.0 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% aqueous ammonia and a brine, and dried over anhydrous magnesium sulfate. The solvent was then removed under reduced pressure to give the title compound (0.83 g, 47%) as white crystal.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07129367B2
出典データセットuspto-grants-2006_10
ORD IDord-aec168b5a6f641b3bf59928e3e57392e
出典メモuspto-grants-2006_10