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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 9790Erstellt: 23. Oktober 2026

Triphenylphosphine → 3-Octene, 1-bromo-, (3Z)-

https://huagongshe.com/de/reaction/9790

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriphenylphosphineHCID 11776—
EduktN-bromobutanimideHCID 67184—
Edukt3-Octen-1-ol, (3Z)-HCID 5364519—
LösungsmittelDimethylformamideHCID 6228—
Produkt3-Octene, 1-bromo-, (3Z)-HCID 643704691,1%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

To a solution of cis-oct-3-en-1-ol (1.00 g, 7.81 mmol) in DMF (18 mL) was added triphenylphosphine (2.28 g, 8.69 mmol). The solution was cooled to 0° C. and NBS (1.50 g, 8.43 mmol) was added in portions. After stirring for 30 min at room temperature, the reaction was quenched with methanol (1 mL). The solution was diluted with ether (100 mL), washed with water, saturated aqueous NaHCO3 and brine successively. The organic layer was dried and concentrated. The residue was purified by flash chromatography on silica gel, eluting with hexane to afford cis-1-bromo-oct-3-ene (1.36 g, 91%) as a colorless oil: 1H NMR (300 MHz, CDCl3) δ 5.53 (1H, m), 5.35 (1H, m), 3.36 (2H, t, J=7.2 Hz), 2.60 (2H, m), 2.04 (2H, m), 1.33 (4H, m), 0.89 (3H, t, J=7.2 Hz); 3C NMR (75 MHz, CDCl3) δ 133.27, 125.84, 32.93, 31.97, 31.12, 27.43, 22.64, 14.30.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07091357B2
Quelldatensatzuspto-grants-2006_08
ORD IDord-3dadb7fa34ef4294929d576b1cfc5657
Quellennotizuspto-grants-2006_08