Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 9814Generated: October 26, 2026

Triphenylphosphine → 1-Bromooct-3-yne

https://huagongshe.com/reaction/9814

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantN-bromobutanimideHCID 67184—
Reactant3-Octyn-1-olHCID 84694—
SolventDimethylformamideHCID 6228—
Product1-Bromooct-3-yneHCID 1247620671.4%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of oct-3-yn-1-ol (1.26 g, 10.0 mmol) in DMF (25 mL) was added triphenylphosphine (2.92 g, 11.2 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 (150 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-oct-3-yne (1.35 g, 71%) as a colorless oil: 1H NMR (300 MHz, CDCl3) δ 3.40 (2H, d, J=7.2 Hz), 2.78 (2H, m), 2.15 (2H, m), 1.22 (4H, m), 0.88 (3H, t, J=6.9 Hz); 13C NMR (75 MHz, CDCl3) δ 82.83, 77.05, 31.18, 30.63, 23.68, 22.20, 18.67, 13.89.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07091357B2
Source datasetuspto-grants-2006_08
ORD IDord-d45dd811ad1242be89b10cf1539f2c95
Source noteuspto-grants-2006_08