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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 551342Erstellt: 25. Oktober 2026

1-Bromonaphthalene → 1-Cyclopropylnaphthalene

https://huagongshe.com/reaction/551342

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
PatentnummerUS07947721B2
Quelldatensatzuspto-grants-2011_05
ORD IDord-13db7488c62f433e84dcd70a8261dcfa
Quellennotizuspto-grants-2011_05