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HRID 1267113作成日:2026年10月25日

1-Iodo-3-nitrobenzene → Tert-butyl 4-(3-nitrophenyl)piperazine-1-carboxylate

https://huagongshe.com/reaction/1267113

反応式

関与物質

役割名称HCID仕込み量
反応物1-Iodo-3-nitrobenzeneHCID 12574—
反応物Tri-o-tolylphosphineHCID 80271—
反応物tert-Butyl piperazine-1-carboxylateHCID 143452—
反応物Sodium t-butoxideHCID 23676156—
触媒Bis(dibenzylideneacetone)palladiumHCID 9811564—
溶媒Diethyl EtherHCID 3283—
溶媒1,4-DioxaneHCID 31275—
生成物Tert-butyl 4-(3-nitrophenyl)piperazine-1-carboxylateHCID 2233012654%

反応手順

To a solution of 1-iodo-3-nitro-benzene (9 g), piperazine-1-carboxylic acid tert-butyl ester (13.5 g) and sodium tert-butoxide (9.7 g) in dioxane (150 mL) was added tris(dibenzylideneacetone)dipalladium (2 g) and tri-o-tolylphosphine (2.2 g) and the mixture was heated at reflux for 24 hours. The solution was then cooled to room temperature, taken in Et2O and washed with brine. The organic layer was dried over Na2SO4, filtered and concentrated under reduced pressure. The crude residue was recrystallized from diisopropyl ether to give the title compound (6 g) as a yellow solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06552022B1
出典データセットuspto-grants-2003_04
ORD IDord-3e6f4f4adc4544aa9e6884a8a24e610d
出典メモuspto-grants-2003_04