HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 9788Erstellt: 25. Oktober 2026
Triphenylphosphine → trans-1-Bromo-dec-4-ene
https://huagongshe.com/reaction/9788
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Triphenylphosphine | HCID 11776 | — |
| Edukt | N-bromobutanimide | HCID 67184 | — |
| Edukt | Dec-4-en-1-ol | HCID 5702619 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | trans-1-Bromo-dec-4-ene | HCID 11160306 | 75% |
Reaktionsschritte
To a solution of trans-dec-4-en-1-ol (1.52 g, 9.74 mmol) in DMF (25 mL) was added triphenylphosphine (2.81 g, 10.7 mmol). The solution was cooled to 0° C. and NBS (1.85 g, 10.4 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-dec-4-ene (1.60 g, 75%) as a colorless oil: 1H NMR (300 MHz, CDCl3) δ 5.49 (1H, m), 5.35 (1H, m), 3.42 (2H, t, J=6.6 Hz), 2.15 (2H, m), 1.96 (4H, m), 1.29 (6H, m), 0.90 (3H, t, J=7.2 Hz); 13C NMR (75 MHz, CDCl3) δ 132.36, 127.89, 33.61, 32.80, 32.73, 31.65, 31.14, 29.45, 22.82, 14.36.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07091357B2 |
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| Quelldatensatz | uspto-grants-2006_08 |
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| ORD ID | ord-8e72ef16052e45c89ba94b6b658974be |
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| Quellennotiz | uspto-grants-2006_08 |
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