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HRID 724633作成日:2026年10月26日

1,1'-Biphenyl, 4-(bromomethyl)- → 1-(2-Biphenyl-4-yl-1-phenyl-ethyl)-1H-benzotriazole

https://huagongshe.com/reaction/724633

反応式

関与物質

役割名称HCID仕込み量
反応物1,1'-Biphenyl, 4-(bromomethyl)-HCID 257716—
反応物1-Benzyl-1H-benzotriazoleHCID 521212—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
生成物1-(2-Biphenyl-4-yl-1-phenyl-ethyl)-1H-benzotriazoleHCID 2187951383%

反応条件

温度-78 °C

反応手順

A solution of 1-benzyl-1H-1,2,3-benzotriazole (750 mg, 3.6 mmol) in tetrahydrofuran (36 mL) was cooled to −78° C. and treated with n-butyllithium (2.8 mL, 1.6 M in hexanes) dropwise. The reaction mixture was stirred at −78° C. for 10 min and 4-bromomethyl-biphenyl (1.0 g, 4.1 mmol) in tetrahydrofuran (4 mL) was added dropwise. The reaction mixture was stirred at −78° C. for 1 h, quenched with sat. ammonium chloride (100 mL), and extracted with ethyl acetate (150 mL). The organic layer was separated and washed with brine (50 mL), dried with sodium sulfate, filtered, and concentrated to a white solid. This material was triturated with diethyl ether (2×50 mL) to yield the desired product (1.12 g, 83%). LCMS found for C26H22N3 (M+H)+: m/z=376.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07141596B2
出典データセットuspto-grants-2006_11
ORD IDord-1d742bfcfbad42edb21b57e3f9c1a024
出典メモuspto-grants-2006_11