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HRID 634557作成日:2026年10月26日

Tris(1,1-dimethylethyl)phosphine → 9-[3-(4,6-Diphenylpyrimidin-2-yl)phenyl]-9'-phenyl-9H,9'H-[3,3]bicarbazolyl

https://huagongshe.com/reaction/634557

反応式

関与物質

役割名称HCID仕込み量
反応物Tris(1,1-dimethylethyl)phosphineHCID 83681—
反応物Sodium t-butoxideHCID 23676156—
反応物2-(3-Bromophenyl)-4,6-diphenylpyrimidineHCID 58943181—
反応物9-Phenyl-9H,9'H-[3,3']bicarbazolylHCID 59306629—
触媒palladium(II) acetateHCID 167845—
溶媒P-XyleneHCID 7809—
生成物9-[3-(4,6-Diphenylpyrimidin-2-yl)phenyl]-9'-phenyl-9H,9'H-[3,3]bicarbazolylHCID 58511489—

反応手順

22.00 g (53.86 mmol) of 9-phenyl-9H,9′H-[3,3′]bicarbazolyl 26, 22.93 g (59.24 mmol) of 2-(3-bromophenyl)-4,6-diphenylpyrimidine 14 and 15.81 g (164.47 mmol) of NaOtBu are suspended in 820 ml of p-xylene. 244.79 mg (1.09 mmol) of Pd(OAc)2 and 3.3 ml of a 1M tri-tert-butylphosphine solution are added to this suspension. The reaction mixture is heated under reflux for 19 h. After cooling, the organic phase is separated off, washed three times with 100 ml of water and subsequently evaporated to dryness. The residue is extracted with hot toluene, recrystallised from toluene and finally sublimed in a high vacuum. The yield is 23.10 g (60%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09324954B2
出典データセットuspto-grants-2016_04
ORD IDord-6adf938bce554fbb8bc9c7ee97c9dd54
出典メモuspto-grants-2016_04