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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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAllyl bromideHCID 7841—
EduktSodium hydrideHCID 24758—
Edukt(-)-1-(4-Fluorophenyl)ethanolHCID 852997—
LösungsmittelDimethylformamideHCID 6228—
Produkt1-((S)-1-allyloxy-ethyl)-4-fluoro-benzeneHCID 6670596080%

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09132136B2
Quelldatensatzuspto-grants-2015_09
ORD IDord-74ccacda75ef4b36acfee4bf7b142e12
Quellennotizuspto-grants-2015_09