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HRID 448138作成日:2026年10月25日

1-Bromonaphthalene → 1-Cyclopropylnaphthalene

https://huagongshe.com/reaction/448138

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, 0.5 M in tetrahydrofuran) was slowly added to a solution of 1-bromo-naphthalene (10 g, 50 mmol) and [1,3-bis(diphenylphosphino)propane]dichloronickel(II) in tetrahydrofuran (10 mL) stirred at 0° C. The reaction mixture was stirred at room temperature for 16 hours and the solvent was evaporated under reduced pressure. EtOAc and ammonium chloride in water 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-cyclopropyl-naphthalene (6.4 g, 76%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08481581B2
出典データセットuspto-grants-2013_07
ORD IDord-ccdd59be48a541a9a605a6921766dcd4
出典メモuspto-grants-2013_07