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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 9823Erstellt: 23. Oktober 2026

Triphenylphosphine → 1-Bromo-7-methyloctane

https://huagongshe.com/de/reaction/9823

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriphenylphosphineHCID 11776—
EduktIsononanolHCID 17072—
EduktN-bromobutanimideHCID 67184—
LösungsmittelDimethylformamideHCID 6228—
Produkt1-Bromo-7-methyloctaneHCID 1363478174,2%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

To a solution of 7-methyl-octan-1-ol (1.20 g, 8.33 mmol) in DMF (20 mL) was added triphenylphosphine (2.43 g, 9.26 mmol). The solution was cooled to 0° C. and NBS (1.60 g, 8.99 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 1-bromo-7-methyl-octane (1.28 g, 74%) as a colorless oil: 1H NMR (300 MHz, CDCl3) δ 3.41 (2H, t, J=6.6 Hz), 1.85 (2H, m), 1.52 (1H, m), 1.42 (2H, m), 1.28 (4H, m), 1.17 (2H, m), 0.87 (3H, s), 0.85 (3H, s); 13C NMR (75 MHz, CDCl3) δ 39.16, 34.34, 33.14, 29.34, 28.52, 28.24, 27.51, 22.94.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07091357B2
Quelldatensatzuspto-grants-2006_08
ORD IDord-1dcf53a9a79d4a13b5884fe5d9b1212b
Quellennotizuspto-grants-2006_08