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HRID 2269729作成日:2026年10月24日

Triphenylphosphine → 4-(2-Bromoethyl)-1,1'-biphenyl

https://huagongshe.com/ja/reaction/2269729

反応式

関与物質

役割名称HCID仕込み量
反応物TriphenylphosphineHCID 11776—
反応物BromineHCID 24408—
反応物2-[1,1'-Biphenyl]-4-yl-1-ethanolHCID 6424577—
溶媒AcetonitrileHCID 6342—
生成物4-(2-Bromoethyl)-1,1'-biphenylHCID 6424581—

反応手順

Bromine (1.5 ml) was added dropwise to an acetonitrile (60 ml) solution of triphenylphosphine (5 g). After stirring for 5 minutes, an acetonitrile solution (30 ml) of 2-(4-biphenylyl)ethanol (5 g) was added to the reaction mixture. The reaction mixture was stirred at room temperature for one hour and concentrated. Diethyl ether was added to the residue. The supernatant was collected, then dried and concentrated. The residue was purified by silica gel column chromatography (eluent: IPE) to obtain 2-(4-bipenylyl)ethylbromide(6 g). 2-(4-Bipenylyl)ethyl bromide (6 g) was dissolved in methanol (100 ml), which was stirred at 70° C. for 48 hours together with potassium thiocyanate (4.0 g). The reaction mixture was concentrated, and the residue was extracted with ethyl acetate. The organic layer was washed with water, then dried and concentrated. The residue was recrystallized from ethyl acetate-hexane to obtain the entitled compound (4.1 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06329389B1
出典データセットuspto-grants-2001_12
ORD IDord-144927d33aa04b4aac1a23944a2acebe
出典メモuspto-grants-2001_12