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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 448138생성일: 2026년 10월 24일

1-Bromonaphthalene → 1-Cyclopropylnaphthalene

https://huagongshe.com/ko/reaction/448138

반응식

참여 물질

역할이름HCID투입량
반응물1-BromonaphthaleneHCID 7001—
반응물HCID 178418630HCID 178418630—
촉매HCID 178418745HCID 178418745—
용매TetrahydrofuranHCID 8028—
생성물1-CyclopropylnaphthaleneHCID 1466869376%

반응 조건

온도0 °C

반응 단계

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%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08481581B2
출처 데이터셋uspto-grants-2013_07
ORD IDord-ccdd59be48a541a9a605a6921766dcd4
출처 메모uspto-grants-2013_07