HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2276377Erstellt: 26. Oktober 2026
Allyl bromide → 1-((S)-1-allyloxy-ethyl)-4-fluoro-benzene
https://huagongshe.com/reaction/2276377
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Allyl bromide | HCID 7841 | — |
| Edukt | Sodium hydride | HCID 24758 | — |
| Edukt | (-)-1-(4-Fluorophenyl)ethanol | HCID 852997 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | 1-((S)-1-allyloxy-ethyl)-4-fluoro-benzene | HCID 66705960 | 80% |
Reaktionsschritte
To a stirred suspension of sodium hydride (3.14 g, 55% dispersion in oil) in dry DMF (180 ml) under an argon atmosphere was added (S)-1-(4-fluorophenyl)-ethanol (8.41 g, CAS 101219-73-2). Allyl bromide (6.6 ml) was then added dropwise. The reaction mixture was stirred for 30 min at room temperature and was then quenched by addition of water. The mixture was extracted with ethyl acetate twice. The combined organic layers were dried (MgSO4) and concentrated in vacuo. The crude product was purified by column chromatography (SiO2; gradient: heptane/EtOAc) to give 1-((S)-1-allyloxy-ethyl)-4-fluoro-benzene (8.66 g, 80%) as a colourless liquid. 1H NMR (300 MHz, CDCl3, δ ppm): 1.43 (d, J=6.6 Hz, 3H), 3.84 (m, 2H), 4.45 (q, J=6.6 Hz, 1H), 5.15 (dd, J1=10.5 Hz, J2=1.8 Hz, 1H), 5.22 (dd, J1=17.4 Hz, J2=1.8 Hz, 1H), 5.89 (m, 1H), 7.03 (m, 2H), 7.29 (m, 2H).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09132136B2 |
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| Quelldatensatz | uspto-grants-2015_09 |
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| ORD ID | ord-74ccacda75ef4b36acfee4bf7b142e12 |
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| Quellennotiz | uspto-grants-2015_09 |
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