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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 9785Generated: October 27, 2026

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

https://huagongshe.com/reaction/9785

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantN-bromobutanimideHCID 67184—
Reactanttrans-3-Octen-1-olHCID 5364475—
SolventDimethylformamideHCID 6228—
Product3-Octene, 1-bromo-, (3E)-HCID 643704573.3%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of trans-oct-3-en-1-ol (1.28 g, 10.0 mmol) in DMF (25 mL) was added triphenylphosphine (2.92 g, 11.1 mmol). The solution was cooled to 0° C. and NBS (1.92 g, 10.8 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 trans-1-bromo-oct-3-ene (1.40 g, 73%) as a colorless oil: 1H NMR (300 MHz, CDCl3) δ 5.54 (1H, m), 5.39 (1H, m), 3.37 (2H, t, J=7.2 Hz), 2.54 (2H, m), 2.02 (2H, m) 1.34 (4H, m), 0.89 (3H, t, J=7.2 Hz); 13C NMR (75 MHz, CDCl3) δ 134.09, 126.45, 36.34, 33.21, 32.48, 31.73, 22.45, 14.24.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07091357B2
Source datasetuspto-grants-2006_08
ORD IDord-ab1539e727ce4dc0bb73166930e09369
Source noteuspto-grants-2006_08