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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 852759Erstellt: 24. Oktober 2026

Benzyl Bromide → (1R,2S,4R,5S)-5-(Benzyloxy)bicyclo[2.2.1]heptan-2-ol

https://huagongshe.com/de/reaction/852759

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzyl BromideHCID 7498—
EduktTetrahydrofuranHCID 8028—
EduktSodium HydroxideHCID 14798—
Edukt15-Crown-5HCID 36336—
Edukt(1R,2S,4R,5S)-Bicyclo[2.2.1]heptane-2,5-diolHCID 9989289—
Produkt(1R,2S,4R,5S)-5-(Benzyloxy)bicyclo[2.2.1]heptan-2-olHCID 10036335—

Reaktionsbedingungen

Temperatur10 °C

Reaktionsschritte

To a stirred solution of (1R,2S,4R,5S)-bicyclo[2.2.1]-heptane-2,5-diol (1.15 g, 8.97 mmol) and 15-crown-5 (0.054 mL, 0.269 mmol) in tetrahydrofuran (30.0 mL, 8.97 mmol) were added at 10° C. (ice/water bath) finely ground sodium hydroxide (2.15 g, 53.8 mmol) and 1-(bromomethyl)benzene (1.07 mL, 8.97 mmol). After stirring at 10° C. for 3 h, the mixture was stirred at ambient temperature overnight. The mixture was partitioned between EtOAc and water, and the organic portions were washed with brine, and conc. in vacuo. The crude product was purified by flash column chromatography (0 to 80% of ethyl acetate in hexanes). The title compound was obtained as a colorless oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07253196B2
Quelldatensatzuspto-grants-2007_08
ORD IDord-85e37eb0157c4996949a0edff5c7ad62
Quellennotizuspto-grants-2007_08