Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 473272Erstellt: 25. Oktober 2026

1-Bromonaphthalene → 1-Cyclopropylnaphthalene

https://huagongshe.com/reaction/473272

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, 0.5M in tetrahydrofuran) was slowly added to a solution of 1-bromonaphthalene (10 g, 50 mmol) and [1,3-bis(diphenylphosphino)propane]dichloro nickel (II) in tetrahydrofuran (10 mL) stirred at 0° C., and the reaction mixture stirred at room temperature for 16 hours. The solvent was removed under reduced pressure and ethyl acetate and aqueous ammonium chloride 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-cyclopropylnaphthalene (6.4 g, 76%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08633232B2
Quelldatensatzuspto-grants-2014_01
ORD IDord-2ee90082f9c743c4975087720c801f95
Quellennotizuspto-grants-2014_01