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HRID 32650作成日:2026年10月25日

Tri-o-tolylphosphine → 1-[2-Chloro-4-(trifluoromethyl)phenyl]piperazine

https://huagongshe.com/reaction/32650

反応式

関与物質

役割名称HCID仕込み量
反応物Tri-o-tolylphosphineHCID 80271—
反応物tert-Butyl piperazine-1-carboxylateHCID 143452—
反応物3-Chloro-4-iodobenzotrifluorideHCID 2736612—
反応物Sodium t-butoxideHCID 23676156—
溶媒Diethyl EtherHCID 3283—
溶媒1,4-DioxaneHCID 31275—
生成物1-[2-Chloro-4-(trifluoromethyl)phenyl]piperazineHCID 4683749610%

反応条件

温度100 °C

反応手順

A mixture of 0.5 g (1.6 mmol) of 3-chloro-4-iodobenzotrifluoride 0.7 g (3.8 mmol), N-Boc-piperazine, 41 mg (0.04 mmol) Tris(dibenzylideneacetone)dipalladium chloroform complex, 0.44 g (4.43 mmol) sodium-t-butoxide and 48 mg (0.16 mmol) tri-o-tolylphosphine in 6 ml dioxane was heated overnight at 100° C. The solution was allowed to cool to room temperature, taken up in ether (30 ml) and washed with brine (25 ml). The organic layer was dried over Na2SO4, filtered and the solvent was removed in vacuo. The crude oil was chromatographed over on silica gel: Eluent: Heptane-AcOEt 0-10% over 15 min to provide the title compound (0.06 g, 10%) as a brown oil, MS (m/e): 365.1 (MH+, 100%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07427612B2
出典データセットuspto-grants-2008_09
ORD IDord-81443adcf32b432695227f565089dcc7
出典メモuspto-grants-2008_09