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HRID 227863作成日:2026年10月26日

Iodine → 2-(Di-tert-butylphosphino)biphenyl

https://huagongshe.com/reaction/227863

反応式

関与物質

役割名称HCID仕込み量
反応物IodineHCID 807—
反応物2-BromobiphenylHCID 16329—
反応物Di-tert-butylchlorophosphineHCID 139566—
反応物MagnesiumHCID 5462224—
溶媒TetrahydrofuranHCID 8028—
生成物2-(Di-tert-butylphosphino)biphenylHCID 273421558%

反応手順

A solution of 2-bromobiphenyl (5.38 g, 23.1 mmol) and a few iodine crystals in 40 mL of THF with magnesium turnings (617 mg, 25.4 mmol) was heated to a reflux for 2 h. Heat was temporarily removed for the addition of cuprous chloride (2.40 g, 24.2 mmol) followed by chlorodi-tert-butylphosphine. Heating was resumed for 8 h. The reaction mixture was then removed from heat and allowed to cool to rt. The reaction mixture was poured onto 200 mL of 1:1 hexane/ether. The suspension was filtered and the filtercake was washed with 60 mL of hexane. The solid was partitioned between 150 mL of 1:1 hexane/ethyl acetate and 60 mL of concentrated ammonium hydroxide with 100 mL of water. The organic layer was washed with 100 mL of brine, dried over anhydrous sodium sulfate, and concentrated in vacuo. The white solid was recrystallized from 30 mL of MeOH to give white crystals of 2-(di-tert-butylphosphino)biphenyl (4.01 g, 58%). A second crop (464 mg, 67%) was obtained by recrystallization from 50 mL of MeOH and 25 mL of water.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07560582B2
出典データセットuspto-grants-2009_07
ORD IDord-98120683f6664ec1ac6c9d02de2e9e8f
出典メモuspto-grants-2009_07