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HRID 551342作成日:2026年10月27日

1-Bromonaphthalene → 1-Cyclopropylnaphthalene

https://huagongshe.com/reaction/551342

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US07947721B2
出典データセットuspto-grants-2011_05
ORD IDord-13db7488c62f433e84dcd70a8261dcfa
出典メモuspto-grants-2011_05