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HRID 7690作成日:2026年10月24日

Benzoyl Peroxide → 5'-(1,3-Benzoxazol-2-yl)-2'-(bromomethyl)-1,1'-biphenyl-3-carbonitrile

https://huagongshe.com/ja/reaction/7690

反応式

関与物質

役割名称HCID仕込み量
反応物Benzoyl PeroxideHCID 7187—
反応物N-bromobutanimideHCID 67184—
反応物5'-(1,3-Benzoxazol-2-yl)-2'-methyl-1,1'-biphenyl-3-carbonitrileHCID 21990975—
溶媒Carbon TetrachlorideHCID 5943—
生成物5'-(1,3-Benzoxazol-2-yl)-2'-(bromomethyl)-1,1'-biphenyl-3-carbonitrileHCID 21990971—

反応手順

A mixture of 5′-(1,3-benzoxazol-2-yl)-2′-methyl-1,1′-biphenyl-3-carbonitrile (229 mg, 0.74 mmol), n-bromosuccinimide (145 mg, 0.81 mmol), and benzoyl peroxide (9 mg, 0.037 mmol) in carbon tetrachloride (15 mL) was refluxed for 5 h. The solvent was evaporated to dryness and the crude was purified by flash chromatography on silica gel eluting with a gradient of EtOAc:hexanes (0 to 30 min: 0 to 20% EtOAc, 30 to 40 min: 50% EtOAc) to afford 5′-(1,3-benzoxazol-2-yl)-2′-(bromomethyl)-1,1′-biphenyl-3-carbonitrile as a colorless solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07087601B2
出典データセットuspto-grants-2006_08
ORD IDord-e5f24134709a4e5289eb9e087aef7de8
出典メモuspto-grants-2006_08