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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 448138Erstellt: 24. Oktober 2026

1-Bromonaphthalene → 1-Cyclopropylnaphthalene

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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-BromonaphthaleneHCID 7001—
EduktHCID 178418630HCID 178418630—
KatalysatorHCID 178418745HCID 178418745—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt1-CyclopropylnaphthaleneHCID 1466869376%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

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%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08481581B2
Quelldatensatzuspto-grants-2013_07
ORD IDord-ccdd59be48a541a9a605a6921766dcd4
Quellennotizuspto-grants-2013_07