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HRID 473272作成日:2026年10月27日

1-Bromonaphthalene → 1-Cyclopropylnaphthalene

https://huagongshe.com/reaction/473272

反応式

関与物質

役割名称HCID仕込み量
反応物1-BromonaphthaleneHCID 7001—
反応物HCID 178418630HCID 178418630—
触媒HCID 178418745HCID 178418745—
溶媒TetrahydrofuranHCID 8028—
生成物1-CyclopropylnaphthaleneHCID 1466869376%

反応条件

温度0 °C

反応手順

Cyclopropylmagnesium bromide (150 mL, 0.5M in tetrahydrofuran) was slowly added to a solution of 1-bromonaphthalene (10 g, 50 mmol) and [1,3-bis(diphenylphosphino)propane]dichloro nickel (II) in tetrahydrofuran (10 mL) stirred at 0° C., and the reaction mixture stirred at room temperature for 16 hours. The solvent was removed under reduced pressure and ethyl acetate and aqueous ammonium chloride were added. After extraction, the organic layer was dried over sodium sulfate, filtered and concentrated under reduced pressure. The residue was purified by silica gel chromatography to yield 1-cyclopropylnaphthalene (6.4 g, 76%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08633232B2
出典データセットuspto-grants-2014_01
ORD IDord-2ee90082f9c743c4975087720c801f95
出典メモuspto-grants-2014_01