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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1736477Erstellt: 24. Oktober 2026

1,2-Bis(diphenylphosphino)ethane → (Cyclopent-2-en-1-yl)benzene

https://huagongshe.com/de/reaction/1736477

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,2-Bis(diphenylphosphino)ethaneHCID 74267—
EduktAcetic acid, cyclopent-2-en-1-yl esterHCID 140735—
EduktHCID 178418255HCID 178418255—
Katalysator1,5-Diphenylpenta-1,4-dien-3-one;palladiumHCID 154270—
KatalysatorZincchlorideHCID 3007855—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt(Cyclopent-2-en-1-yl)benzeneHCID 142190—

Reaktionsbedingungen

Temperatur40 °C

Reaktionsschritte

A solution of 8 mL of 2M phenylmagnesium bromide in THF was added dropwise to a solution of 32.2 mL (0.016 mole) of 0.5M zinc chloride in THF. A solution of 3.05g (0.024 mole) of 3-acetoxycyclopent-1-ene in 25 mL of dry THF was added, and 321 mg of 1,2-bis(diphenylphosphino)ethane and 462 mg of palladium bis(dibenzylideneacetone) added. The reaction mixture was heated at 40° C. for 18h. The reaction was cooled to room temperature and the solids filtered off. Ether was added, and the organic layer was washed sequentially with saturated ammonium chloride, water, and brine. After drying (MgSO4), the solvent was evaporated in vacuo to give 6 g of a yellow oil. Flash chromatography (SiO2) eluting with hexane gave 760 mg of an oil. Mass spectrum (Cl-NH3) m/z=145 (M+1); 300 MHz NMR (CDCl3) δ 1.68-1.78 (m, 1H); 2.32-2.6 (m, 3H); 3.85-3.96 (m, 1H); 5.72-5.82 (m, 1H); 5.92-6.01 (m, 1H); 7.12-7.38 (m, 5H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05541217
Quelldatensatzuspto-grants-1996_07
ORD IDord-0bbff7524b774ea89cdb78632010a69b
Quellennotizuspto-grants-1996_07