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HRID 401148作成日:2026年10月26日

Benzene, 1-bromo-3,5-dichloro- → 1-(3,5-Dichlorophenyl)-2-phenylethanone

https://huagongshe.com/reaction/401148

反応式

関与物質

役割名称HCID仕込み量
反応物Benzene, 1-bromo-3,5-dichloro-HCID 29766—
反応物2-(3-Methylphenyl)acetophenoneHCID 13173614—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
生成物1-(3,5-Dichlorophenyl)-2-phenylethanoneHCID 275814619.4%

反応手順

To a solution of 1-bromo-3,5-dichlorobenzene (1 g, 4.4 mmol) in anhydrous THF (10 mL) was added n-BuLi (339 mg, 5.3 mmol) at −78° C. After being stirred for 30 minutes, a solution of N-methoxy-N-methyl-2-phenyl-acetamide (prepared following step 1 of Intermediate 4) (790 mg, 4.4 mmol) in THF (5 mL) was added, and the mixture was stirred for 3 hours. When TLC indicated that starting material was consumed, the reaction mixture was diluted with water (50 mL), and extracted with EtOAc (20 mL×3). The combined organic layer was dried over Na2SO4, concentrated in vacuum, and purified by column chromatography (PE: EtOAc=50:1) to afford 1-(3,5-dichlorophenyl)-2-phenylethanone (213 mg, yield 19.4%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08741915B2
出典データセットuspto-grants-2014_06
ORD IDord-a41b62129a98498184cf1dd762af7527
出典メモuspto-grants-2014_06