HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 9785Generated: October 27, 2026
Triphenylphosphine → 3-Octene, 1-bromo-, (3E)-
https://huagongshe.com/reaction/9785
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | trans-3-Octen-1-ol | HCID 5364475 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-Octene, 1-bromo-, (3E)- | HCID 6437045 | 73.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07091357B2 |
|---|
| Source dataset | uspto-grants-2006_08 |
|---|
| ORD ID | ord-ab1539e727ce4dc0bb73166930e09369 |
|---|
| Source note | uspto-grants-2006_08 |
|---|