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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 502916Erstellt: 27. Oktober 2026

Ethylene Glycol → 3-Bromo-4,4-ethylenedioxy-bicyclo[3.2.1]oct-6-en-2-one

https://huagongshe.com/reaction/502916

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthylene GlycolHCID 174—
EduktSodium GlycolateHCID 517347—
EduktSodiumHCID 5360545—
EduktMonosodium phosphateHCID 23672064—
Edukt3,4-Dibromo-bicyclo[3.2.1]octa-3,6-dien-2-oneHCID 68464392—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelEthyl acetate hexaneHCID 21226206—
ProduktSodium GlycolateHCID 517347—
Produkt3-Bromo-4,4-ethylenedioxy-bicyclo[3.2.1]oct-6-en-2-oneHCID 58609535100%

Reaktionsschritte

A sodium glycolate solution is prepared by stirring 124 mg (5.4 mmol) of metallic sodium into 2.7 ml (42.42 mmol) of anhydrous ethylene glycol at ambient temperature and, when the sodium has completely dissolved, 1.5 ml of tetrahydrofuran are added. To the resulting monosodium glycolate solution there is then added dropwise a solution of 1 g (3.6 mmol) of 3,4-dibromo-bicyclo[3.2.1]octa-3,6-dien-2-one (prepared according to Organic Lett. 4(12), 1997 (2002)) dissolved in 5 ml of tetrahydrofuran. The reaction mixture is then stirred at ambient temperature for 90 minutes with TLC monitoring (mobile phase hexane/ethyl acetate 4:1). The reaction mixture is then treated with 8 ml of 10% sodium dihydrogen phosphate solution and extracted with ethyl acetate (3×). The organic phase is washed with water to remove ethylene glycol, then dried and concentrated by evaporation. 930 mg (˜100%) of 3-bromo-4,4-ethylenedioxy-bicyclo[3.2.1]oct-6-en-2-one are obtained in the form of a white solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07776888B2
Quelldatensatzuspto-grants-2010_08
ORD IDord-305bc184b8f043d1932ca2e25f171f4c
Quellennotizuspto-grants-2010_08